A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176124



Internal ID15855581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112953875..113021309hg38UCSC Ensembl
Innerchr9:115716155..115783589hg19UCSC Ensembl
Innerchr9:114755976..114823410hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3867435
hg1967435
hg1867435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615201
Supporting Variants
Samples1782681114_A
Known GenesZNF883
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176124
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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