A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556592



Internal ID15997315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132994284..133127928hg38UCSC Ensembl
Innerchr11:132864179..132997823hg19UCSC Ensembl
Innerchr11:132369389..132503033hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38133645
hg19133645
hg18133645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785138
Samples
Known GenesOPCML
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556592
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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