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dbVar

Database of genomic structural variation

nsv5566662

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:4,832

Publication(s):Ebert et al. 2021

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: 199 SVs from 44 studies. See in: genome view

Submitted genomic62,214,434-62,219,265

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5566662	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	62,214,434	62,219,265
nsv5566662	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	62,924,339	62,929,170

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17147927	deletion	SAMN00004622	Sequencing	Sequence alignment	1,208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17147927	Submitted genomic		NC_000006.12:g.622 14434_62219265delT	GRCh38 (hg38)		NC_000006.12	Chr6	62,214,434	62,219,265
nssv17147927	Remapped	Perfect	NC_000006.11:g.629 24339_62929170delT	GRCh37.p13	First Pass	NC_000006.11	Chr6	62,924,339	62,929,170

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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