A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589318



Internal ID16030041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1105517..2167148hg38UCSC Ensembl
Innerchr3:1147201..2208832hg19UCSC Ensembl
Innerchr3:1122201..2183832hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381061632
hg191061632
hg181061632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8157n54
Supporting Variantsnssv1152429
SamplesHGDP01374
Known GenesCNTN4, CNTN4-AS2, CNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589318
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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