A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768174



Internal ID15715444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11840666..11854600hg38UCSC Ensembl
Innerchr11:11862213..11876147hg19UCSC Ensembl
Innerchr11:11818789..11832723hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3813935
hg1913935
hg1813935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553534
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)nssv768174
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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