A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145272



Internal ID15651772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131293789..131358182hg38UCSC Ensembl
Innerchr9:134169176..134233569hg19UCSC Ensembl
Innerchr9:133158997..133223390hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3864394
hg1964394
hg1864394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615536
Supporting Variants
Samples
Known GenesPPAPDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145272
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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