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dbVar

Database of genomic structural variation

nsv5581824

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:58

Publication(s):Ebert et al. 2021

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: 120 SVs from 36 studies. See in: genome view

Submitted genomic33,161,196-33,161,253

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5581824	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	33,161,196	33,161,253
nsv5581824	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	33,128,973	33,129,030

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17141992	deletion	HG03683	Sequencing	Sequence alignment	2,232

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17141992	Submitted genomic		NC_000006.12:g.331 61196_33161253delA	GRCh38 (hg38)		NC_000006.12	Chr6	33,161,196	33,161,253
nssv17141992	Remapped	Perfect	NC_000006.11:g.331 28973_33129030delA	GRCh37.p13	First Pass	NC_000006.11	Chr6	33,128,973	33,129,030

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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