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dbVar

Database of genomic structural variation

nsv5901879

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:102

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

Submitted genomic129,976,332-129,976,433

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5901879	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	129,976,332	129,976,433
nsv5901879	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	129,695,175	129,695,276

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17391460	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17391460	Submitted genomic		NC_000003.12:g.129 976332_129976433de l	GRCh38 (hg38)		NC_000003.12	Chr3	129,976,332	129,976,433
nssv17391460	Remapped	Perfect	NC_000003.11:g.129 695175_129695276de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	129,695,175	129,695,276

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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