A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556112



Internal ID16343521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99756622..99780102hg38UCSC Ensembl
Innerchr11:99627353..99650833hg19UCSC Ensembl
Innerchr11:99132563..99156043hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3823481
hg1923481
hg1823481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2130n54
Supporting Variantsnssv781984
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556112
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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