A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768192



Internal ID15715462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11847002..11864294hg38UCSC Ensembl
Innerchr11:11868549..11885841hg19UCSC Ensembl
Innerchr11:11825125..11842417hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3817293
hg1917293
hg1817293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553538
Supporting Variants
Samples
Known GenesUSP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768192
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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