A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785132



Internal ID15732402
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 StatusS
Merged Variantsnsv556587
Supporting Variants
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785132
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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