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dbVar

Database of genomic structural variation

nsv5588287

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:45,572

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: 383 SVs from 50 studies. See in: genome view

Submitted genomic15,162,839-15,208,410

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5588287	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	15,162,839	15,208,410
nsv5588287	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	15,162,838	15,208,409

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17101025	deletion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17101025	Submitted genomic		NC_000018.10:g.151 62839_15208410delT	GRCh38 (hg38)		NC_000018.10	Chr18	15,162,839	15,208,410
nssv17101025	Remapped	Perfect	NC_000018.9:g.1516 2838_15208409delT	GRCh37.p13	First Pass	NC_000018.9	Chr18	15,162,838	15,208,409

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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