A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156457



Internal ID15874976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21455815..21492507hg38UCSC Ensembl
Innerchr9:21455814..21492506hg19UCSC Ensembl
Innerchr9:21445814..21482506hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3836693
hg1936693
hg1836693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613759
Supporting Variants
SamplesHGDP00616
Known GenesIFNE, MIR31HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156457
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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