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dbVar

Database of genomic structural variation

nsv5924410

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:411,850

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: 1409 SVs from 80 studies. See in: genome view

Submitted genomic111,494,845-111,906,694

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5924410	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	111,494,845	111,906,694
nsv5924410	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	114,257,125	114,668,974

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17435275	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17435275	Submitted genomic		NC_000009.12:g.111 494845_111906694de l	GRCh38 (hg38)		NC_000009.12	Chr9	111,494,845	111,906,694
nssv17435275	Remapped	Perfect	NC_000009.11:g.114 257125_114668974de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	114,257,125	114,668,974

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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