A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556587



Internal ID15997310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132165792..132166780hg38UCSC Ensembl
Innerchr11:132035686..132036674hg19UCSC Ensembl
Innerchr11:131540896..131541884hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38989
hg19989
hg18989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785132
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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