A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556589



Internal ID15997312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132454345..132517566hg38UCSC Ensembl
Innerchr11:132324239..132387460hg19UCSC Ensembl
Innerchr11:131829449..131892670hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3863222
hg1963222
hg1863222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785134
Samples
Known GenesOPCML
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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