A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556564



Internal ID15997287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:129908477..129934918hg38UCSC Ensembl
Innerchr11:129778372..129804813hg19UCSC Ensembl
Innerchr11:129283582..129310023hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3826442
hg1926442
hg1826442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176201
SamplesHGDP01021
Known GenesPRDM10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556564
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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