A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv769279



Internal ID15716549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28049932..28117162hg38UCSC Ensembl
Innerchr11:28071479..28138709hg19UCSC Ensembl
Innerchr11:28028055..28095285hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3867231
hg1967231
hg1867231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553915
Supporting Variants
Samples
Known GenesKIF18A, METTL15, MIR610
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv769279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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