A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768173



Internal ID15715443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11840666..11854578hg38UCSC Ensembl
Innerchr11:11862213..11876125hg19UCSC Ensembl
Innerchr11:11818789..11832701hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3813913
hg1913913
hg1813913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553533
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)nssv768173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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