A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695111



Internal ID15431763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15974786..15979115hg38UCSC Ensembl
Innerchr19:16085596..16089925hg19UCSC Ensembl
Innerchr19:15946596..15950925hg18UCSC Ensembl
Innerchr19:15946596..15950925hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg384330
hg194330
hg184330
hg174330
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522331
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695111
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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