A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681119



Internal ID15071085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43009507..43154674hg38UCSC Ensembl
Innerchr19:43513659..43658826hg19UCSC Ensembl
Innerchr19:48205499..48350666hg18UCSC Ensembl
Innerchr19:48205499..48350666hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38145168
hg19145168
hg18145168
hg17145168
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG11, PSG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681119
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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