A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556131



Internal ID15996854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101115046..101609286hg38UCSC Ensembl
Innerchr11:100985777..101480017hg19UCSC Ensembl
Innerchr11:100490987..100985227hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38494241
hg19494241
hg18494241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781995
Samples
Known GenesLOC101054525, MIR3920, PGR, TRPC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556131
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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