A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156456



Internal ID15506626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21391699..21507590hg38UCSC Ensembl
Innerchr9:21391698..21507589hg19UCSC Ensembl
Innerchr9:21381698..21497589hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38115892
hg19115892
hg18115892
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613758
Supporting Variants
Samples1780854081_A
Known GenesIFNA1, IFNA8, IFNE, MIR31HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156456
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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