A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156221



Internal ID15530807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6669474..6786734hg38UCSC Ensembl
Innerchr9:6669474..6786734hg19UCSC Ensembl
Innerchr9:6659474..6776734hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38117261
hg19117261
hg18117261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613212
Supporting Variants
SamplesHGDP00998
Known GenesKDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156221
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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