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dbVar

Database of genomic structural variation

nsv5566966

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:104

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: 132 SVs from 28 studies. See in: genome view

Submitted genomic155,027,283-155,027,386

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5566966	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	155,027,283	155,027,386
nsv5566966	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	154,999,759	154,999,862

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17060972	deletion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17060972	Submitted genomic		NC_000001.11:g.155 027283_155027386de lC	GRCh38 (hg38)		NC_000001.11	Chr1	155,027,283	155,027,386
nssv17060972	Remapped	Perfect	NC_000001.10:g.154 999759_154999862de lC	GRCh37.p13	First Pass	NC_000001.10	Chr1	154,999,759	154,999,862

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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