A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv781956



Internal ID16075912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99621772..99638468hg38UCSC Ensembl
Innerchr11:99492503..99509199hg19UCSC Ensembl
Innerchr11:98997713..99014409hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3816697
hg1916697
hg1816697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556093
Supporting Variants
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv781956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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