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dbVar

Database of genomic structural variation

nsv6131901

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:45,806

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: 392 SVs from 75 studies. See in: genome view

Remapped(Score: Perfect):1,894,034-1,939,839

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv6131901	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	1,894,034	1,894,035	1,939,820	1,939,839
nsv6131901	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	1,915,264	1,915,265	1,961,050	1,961,069

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17681424	inversion	SAMN20524658	Sequencing	Paired-end mapping	48

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17681424	Remapped	Perfect	NC_000011.10:g.(18 94034_1894035)_(19 39820_1939839)inv	GRCh38.p12	First Pass	NC_000011.10	Chr11	1,894,034	1,894,035	1,939,820	1,939,839
nssv17681424	Submitted genomic		NC_000011.9:g.(191 5264_1915265)_(196 1050_1961069)inv	GRCh37 (hg19)		NC_000011.9	Chr11	1,915,264	1,915,265	1,961,050	1,961,069

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

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