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dbVar

Database of genomic structural variation

nsv5591807

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:1,202

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: 154 SVs from 42 studies. See in: genome view

Submitted genomic18,276,646-18,277,847

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5591807	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	18,276,646	18,277,847
nsv5591807	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	18,387,456	18,388,657

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103895	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
nssv17103895	Submitted genomic		NC_000019.10:g.182 76646_18277847delG	GRCh38 (hg38)		NC_000019.10	Chr19	18,276,646	18,277,847
nssv17103895	Remapped	Perfect	NC_000019.9:g.1838 7456_18388657delG	GRCh37.p13	First Pass	NC_000019.9	Chr19	18,387,456	18,388,657

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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