A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615201



Internal ID16402610
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 StatusM
Merged Variants
Supporting Variantsnssv1141244, nssv1176124
Samples1782681114_A
Known GenesZNF883
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615201
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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