A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556166



Internal ID16343575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103079240..103321803hg38UCSC Ensembl
Innerchr11:102949969..103192532hg19UCSC Ensembl
Innerchr11:102455179..102697742hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38242564
hg19242564
hg18242564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv782097
Samples
Known GenesDCUN1D5, DYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556166
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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