nsv6629306

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:49
Validation:Not tested
Clinical Assertions: No
Region Size:116,119

Publication(s):Zarrei et al. 2023

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 1126 SVs from 92 studies. See in: genome view

Remapped(Score: Perfect):75,398,101-75,514,219

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6629306	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nsv6629306	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	75,447,252	75,563,370

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18301538	deletion	OSC5733	SNP array	Probe signal intensity	10
nssv18301578	deletion	OSC5763	SNP array	Probe signal intensity	9
nssv18301599	deletion	OSC5783	SNP array	Probe signal intensity	9
nssv18302419	deletion	OSC5739	SNP array	Probe signal intensity	5
nssv18302538	deletion	OSC5852	SNP array	Probe signal intensity	15
nssv18303059	deletion	OSC5998	SNP array	Probe signal intensity	11
nssv18303346	deletion	OSC5965	SNP array	Probe signal intensity	12
nssv18303426	deletion	OSC6017	SNP array	Probe signal intensity	7
nssv18303555	deletion	OSC5919	SNP array	Probe signal intensity	11
nssv18303558	deletion	OSC5920	SNP array	Probe signal intensity	11
nssv18303607	deletion	OSC5961	SNP array	Probe signal intensity	5
nssv18304074	deletion	OSC6238	SNP array	Probe signal intensity	10
nssv18304126	deletion	OSC6106	SNP array	Probe signal intensity	10
nssv18304164	deletion	OSC6147	SNP array	Probe signal intensity	11
nssv18304237	deletion	OSC6189	SNP array	Probe signal intensity	8
nssv18304318	deletion	OSC6236	SNP array	Probe signal intensity	12
nssv18304533	deletion	OSC6155	SNP array	Probe signal intensity	8
nssv18304804	deletion	OSC6144	SNP array	Probe signal intensity	6
nssv18304829	deletion	OSC6153	SNP array	Probe signal intensity	9
nssv18304889	deletion	OSC6190	SNP array	Probe signal intensity	9
nssv18304931	deletion	OSC6223	SNP array	Probe signal intensity	13
nssv18305102	deletion	OSC6325	SNP array	Probe signal intensity	9
nssv18305351	deletion	OSC6329	SNP array	Probe signal intensity	13
nssv18305732	deletion	OSC6356	SNP array	Probe signal intensity	9
nssv18305743	deletion	OSC6361	SNP array	Probe signal intensity	11
nssv18305754	deletion	OSC6376	SNP array	Probe signal intensity	11
nssv18306483	deletion	OSC6623	SNP array	Probe signal intensity	5
nssv18308267	deletion	OSC6829	SNP array	Probe signal intensity	7
nssv18308941	deletion	OSC7044	SNP array	Probe signal intensity	8
nssv18310036	deletion	OSC7142	SNP array	Probe signal intensity	11
nssv18310073	deletion	OSC7166	SNP array	Probe signal intensity	10
nssv18310478	deletion	OSC7287	SNP array	Probe signal intensity	9
nssv18310556	deletion	OSC7356	SNP array	Probe signal intensity	8
nssv18310560	deletion	OSC7359	SNP array	Probe signal intensity	11
nssv18312000	deletion	OSC7480	SNP array	Probe signal intensity	23
nssv18312031	deletion	OSC7499	SNP array	Probe signal intensity	7
nssv18312252	deletion	OSC7475	SNP array	Probe signal intensity	6
nssv18312278	deletion	OSC7496	SNP array	Probe signal intensity	13
nssv18312641	deletion	OSC7762	SNP array	Probe signal intensity	9
nssv18312726	deletion	OSC7811	SNP array	Probe signal intensity	11
nssv18315077	deletion	OSC8142	SNP array	Probe signal intensity	nssv18315075, nssv18315076
nssv18316448	deletion	OSC8183	SNP array	Probe signal intensity	13
nssv18316890	deletion	OSC8306	SNP array	Probe signal intensity	9
nssv18317268	deletion	OSC8380	SNP array	Probe signal intensity	10
nssv18319491	deletion	OSC8805	SNP array	Probe signal intensity	12
nssv18319732	deletion	OSC8781	SNP array	Probe signal intensity	8
nssv18320476	deletion	OSC8838	SNP array	Probe signal intensity	nssv18320205, nssv18320475
nssv18320506	deletion	OSC8864	SNP array	Probe signal intensity	7
nssv18320751	deletion	OSC8841	SNP array	Probe signal intensity	10

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18301538	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18301578	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18301599	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18302419	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18302538	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18303059	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18303346	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18303426	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18303555	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18303558	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18303607	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304074	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304126	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304164	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304237	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304318	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304533	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304804	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304829	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304889	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18304931	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18305102	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18305351	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18305732	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18305743	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18305754	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18306483	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18308267	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18308941	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18310036	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18310073	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18310478	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18310556	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18310560	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18312000	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18312031	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18312252	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18312278	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18312641	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18312726	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18315077	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18316448	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18316890	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18317268	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18319491	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18319732	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18320476	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18320506	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18320751	Remapped	Perfect	NC_000003.12:g.(?_ 75398101)_(7551421 9_?)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	75,398,101	75,514,219
nssv18301538	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18301578	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18301599	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18302419	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18302538	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18303059	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18303346	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18303426	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18303555	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18303558	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18303607	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304074	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304126	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304164	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304237	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304318	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304533	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304804	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304829	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304889	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18304931	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18305102	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18305351	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18305732	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18305743	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18305754	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18306483	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18308267	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18308941	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18310036	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18310073	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18310478	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18310556	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18310560	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18312000	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18312031	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18312252	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18312278	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18312641	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18312726	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18315077	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18316448	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18316890	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18317268	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18319491	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18319732	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18320476	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18320506	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370
nssv18320751	Submitted genomic		NC_000003.11:g.(?_ 75447252)_(7556337 0_?)del	GRCh37 (hg19)		NC_000003.11	Chr3	75,447,252	75,563,370

dbVar

Database of genomic structural variation

nsv6629306

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant