A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615225



Internal ID16055948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114064562..114104774hg38UCSC Ensembl
Innerchr9:116826842..116867054hg19UCSC Ensembl
Innerchr9:115866663..115906875hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3840213
hg1940213
hg1840213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12855n54
Supporting Variantsnssv1176466, nssv1176465
SamplesHGDP00604, HGDP00572
Known GenesAMBP, KIF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615225
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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