A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176209



Internal ID15526070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134288851..134327741hg38UCSC Ensembl
Innerchr11:134158745..134197635hg19UCSC Ensembl
Innerchr11:133663955..133702845hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3838891
hg1938891
hg1838891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556604
Supporting Variants
SamplesHGDP00031
Known GenesGLB1L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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