A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174951



Internal ID15532656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103066950..103185951hg38UCSC Ensembl
Innerchr11:102937679..103056680hg19UCSC Ensembl
Innerchr11:102442889..102561890hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38119002
hg19119002
hg18119002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556165
Supporting Variants
SamplesHGDP01348
Known GenesDCUN1D5, DYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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