A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1130800



Internal ID15983986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21170365..21216029hg38UCSC Ensembl
Innerchr9:21170364..21216028hg19UCSC Ensembl
Innerchr9:21160364..21206028hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3845665
hg1945665
hg1845665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613755
Supporting Variants
Samples
Known GenesIFNA10, IFNA4, IFNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1130800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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