A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176460



Internal ID15528051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114053497..114104774hg38UCSC Ensembl
Innerchr9:116815777..116867054hg19UCSC Ensembl
Innerchr9:115855598..115906875hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3851278
hg1951278
hg1851278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615224
Supporting Variants
SamplesHGDP00582
Known GenesAMBP, KIF12, ZNF618
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176460
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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