A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556594



Internal ID15997317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133486593..133656068hg38UCSC Ensembl
Innerchr11:133356488..133525963hg19UCSC Ensembl
Innerchr11:132861698..133031173hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38169476
hg19169476
hg18169476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785140
Samples
Known GenesOPCML
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556594
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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