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dbVar

Database of genomic structural variation

nsv5923794

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:132

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: 156 SVs from 41 studies. See in: genome view

Submitted genomic90,841,466-90,841,597

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5923794	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	90,841,466	90,841,597
nsv5923794	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	93,603,748	93,603,879

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17437101	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17437101	Submitted genomic		NC_000009.12:g.908 41466_90841597del	GRCh38 (hg38)		NC_000009.12	Chr9	90,841,466	90,841,597
nssv17437101	Remapped	Perfect	NC_000009.11:g.936 03748_93603879del	GRCh37.p13	First Pass	NC_000009.11	Chr9	93,603,748	93,603,879

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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