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dbVar

Database of genomic structural variation

nsv6635468

Organism: Homo sapiens

Study:nstd227 (Kikas et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:73,444

Publication(s):Kikas 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: 446 SVs from 69 studies. See in: genome view

Remapped(Score: Perfect):14,945,441-15,018,884

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv6635468	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	14,945,441	15,018,884
nsv6635468	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	14,987,440	15,060,883

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18326949	deletion	SNP array	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv18326949	Remapped	Perfect	NC_000010.11:g.(14 945441_?)_(?_15018 884)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	14,945,441	15,018,884
nssv18326949	Submitted genomic		NC_000010.10:g.(14 987440_?)_(?_15060 883)del	GRCh37 (hg19)		NC_000010.10	Chr10	14,987,440	15,060,883

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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