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dbVar

Database of genomic structural variation

nsv5917367

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:199

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

Submitted genomic32,162,606-32,162,804

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5917367	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	32,162,606	32,162,804
nsv5917367	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	32,020,122	32,020,320

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17444436	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17444436	Submitted genomic		NC_000008.11:g.321 62606_32162804del	GRCh38 (hg38)		NC_000008.11	Chr8	32,162,606	32,162,804
nssv17444436	Remapped	Perfect	NC_000008.10:g.320 20122_32020320del	GRCh37.p13	First Pass	NC_000008.10	Chr8	32,020,122	32,020,320

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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