A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174807



Internal ID15506752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63465891..63552767hg38UCSC Ensembl
Innerchr11:63233363..63320239hg19UCSC Ensembl
Innerchr11:62989939..63076815hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3886877
hg1986877
hg1886877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555179
Supporting Variants
Samples1780854205_A
Known GenesHRASLS5, LGALS12, MIR3680-1, MIR3680-2, RARRES3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174807
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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