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dbVar

Database of genomic structural variation

nsv5916791

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:184

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: 118 SVs from 22 studies. See in: genome view

Submitted genomic97,896,725-97,896,908

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5916791	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	97,896,725	97,896,908
nsv5916791	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	100,659,007	100,659,190

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17438817	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17438817	Submitted genomic		NC_000009.12:g.978 96725_97896908del	GRCh38 (hg38)		NC_000009.12	Chr9	97,896,725	97,896,908
nssv17438817	Remapped	Perfect	NC_000009.11:g.100 659007_100659190de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	100,659,007	100,659,190

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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