A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv781729



Internal ID16075685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99236286..99289771hg38UCSC Ensembl
Innerchr11:99107017..99160502hg19UCSC Ensembl
Innerchr11:98612227..98665712hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3853486
hg1953486
hg1853486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556057
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)nssv781729
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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