A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156735



Internal ID15879680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15641281..15726059hg38UCSC Ensembl
Innerchr9:15641279..15726057hg19UCSC Ensembl
Innerchr9:15631279..15716057hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3884779
hg1984779
hg1884779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613659
Supporting Variants
SamplesHGDP01415
Known GenesCCDC171
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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