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dbVar

Database of genomic structural variation

nsv5903997

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:148

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: 137 SVs from 41 studies. See in: genome view

Submitted genomic126,949,482-126,949,629

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5903997	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	126,949,482	126,949,629
nsv5903997	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	126,668,325	126,668,472

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17405859	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17405859	Submitted genomic		NC_000003.12:g.126 949482_126949629de l	GRCh38 (hg38)		NC_000003.12	Chr3	126,949,482	126,949,629
nssv17405859	Remapped	Perfect	NC_000003.11:g.126 668325_126668472de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	126,668,325	126,668,472

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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