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dbVar

Database of genomic structural variation

nsv5901901

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:457

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

Submitted genomic37,032,164-37,032,620

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5901901	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	37,032,164	37,032,620
nsv5901901	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	37,073,655	37,074,111

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17414135	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17414135	Submitted genomic		NC_000003.12:g.370 32164_37032620del	GRCh38 (hg38)		NC_000003.12	Chr3	37,032,164	37,032,620
nssv17414135	Remapped	Perfect	NC_000003.11:g.370 73655_37074111del	GRCh37.p13	First Pass	NC_000003.11	Chr3	37,073,655	37,074,111

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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