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dbVar

Database of genomic structural variation

nsv5565158

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:324

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: 160 SVs from 51 studies. See in: genome view

Submitted genomic231,131,462-231,131,785

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5565158	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	231,131,462	231,131,785
nsv5565158	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	231,996,176	231,996,499

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17111794	deletion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17111794	Submitted genomic		NC_000002.12:g.231 131462_231131785de lT	GRCh38 (hg38)		NC_000002.12	Chr2	231,131,462	231,131,785
nssv17111794	Remapped	Perfect	NC_000002.11:g.231 996176_231996499de lT	GRCh37.p13	First Pass	NC_000002.11	Chr2	231,996,176	231,996,499

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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