A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766330



Internal ID15713600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6601484..6647097hg38UCSC Ensembl
Innerchr11:6622714..6668328hg19UCSC Ensembl
Innerchr11:6579290..6624904hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3845614
hg1945615
hg1845615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553373
Supporting Variants
Samples
Known GenesDCHS1, ILK, RRP8, TAF10, TPP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv766330
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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