A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659196



Internal ID15395848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41477914..41495302hg38UCSC Ensembl
Innerchr19:41983822..42001210hg19UCSC Ensembl
Innerchr19:46675662..46693050hg18UCSC Ensembl
Innerchr19:46675662..46693050hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3817389
hg1917389
hg1817389
hg1717389
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519523
Supporting Variants
Samples
Known GenesLOC100505495
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659196
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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