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dbVar

Database of genomic structural variation

nsv5579727

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: 139 SVs from 26 studies. See in: genome view

Submitted genomic201,924,395-201,924,498

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5579727	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	201,924,395	201,924,498
nsv5579727	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	201,893,523	201,893,626

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17062424	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
nssv17062424	Submitted genomic		NC_000001.11:g.201 924395_201924498de lA	GRCh38 (hg38)		NC_000001.11	Chr1	201,924,395	201,924,498
nssv17062424	Remapped	Perfect	NC_000001.10:g.201 893523_201893626de lA	GRCh37.p13	First Pass	NC_000001.10	Chr1	201,893,523	201,893,626

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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