A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556120



Internal ID16343529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99907474..99939215hg38UCSC Ensembl
Innerchr11:99778206..99809947hg19UCSC Ensembl
Innerchr11:99283416..99315157hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3831742
hg1931742
hg1831742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781989
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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