A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656972



Internal ID15393624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28901839..28905720hg38UCSC Ensembl
Innerchr19:29392746..29396627hg19UCSC Ensembl
Innerchr19:34084586..34088467hg18UCSC Ensembl
Innerchr19:34084586..34088467hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg383882
hg193882
hg183882
hg173882
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517098
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656972
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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