A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156225



Internal ID15855339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7030268..7084558hg38UCSC Ensembl
Innerchr9:7030268..7084558hg19UCSC Ensembl
Innerchr9:7020268..7074558hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3854291
hg1954291
hg1854291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613258
Supporting Variants
Samples1780862573_A
Known GenesKDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156225
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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