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dbVar

Database of genomic structural variation

nsv5921627

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:578

Publication(s):Almarri et al. 2020

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: 142 SVs from 25 studies. See in: genome view

Submitted genomic60,577,084-60,577,661

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5921627	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	60,577,084	60,577,661
nsv5921627	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	61,489,643	61,490,220

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17441649	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17441649	Submitted genomic		NC_000008.11:g.605 77084_60577661del	GRCh38 (hg38)		NC_000008.11	Chr8	60,577,084	60,577,661
nssv17441649	Remapped	Perfect	NC_000008.10:g.614 89643_61490220del	GRCh37.p13	First Pass	NC_000008.10	Chr8	61,489,643	61,490,220

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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