A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778991



Internal ID15726261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72573525..72625520hg38UCSC Ensembl
Innerchr11:72284569..72336564hg19UCSC Ensembl
Innerchr11:71962217..72014212hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3851996
hg1951996
hg1851996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555407
Supporting Variants
Samples
Known GenesMIR139, PDE2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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