A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556113



Internal ID16343522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99758241..99780102hg38UCSC Ensembl
Innerchr11:99628972..99650833hg19UCSC Ensembl
Innerchr11:99134182..99156043hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3821862
hg1921862
hg1821862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2130n54
Supporting Variantsnssv1174938
Samples1780862310_A
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556113
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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