A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174762



Internal ID15853873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24947682..25039801hg38UCSC Ensembl
Innerchr11:24969228..25061347hg19UCSC Ensembl
Innerchr11:24925804..25017923hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3892120
hg1992120
hg1892120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553828
Supporting Variants
Samples1780854464_A
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174762
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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