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dbVar

Database of genomic structural variation

nsv5925709

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:294

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: 143 SVs from 23 studies. See in: genome view

Submitted genomic121,964,397-121,964,690

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5925709	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	121,964,397	121,964,690
nsv5925709	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	123,723,912	123,724,205

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17357097	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17357097	Submitted genomic		NC_000010.11:g.121 964397_121964690de l	GRCh38 (hg38)		NC_000010.11	Chr10	121,964,397	121,964,690
nssv17357097	Remapped	Perfect	NC_000010.10:g.123 723912_123724205de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	123,723,912	123,724,205

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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