A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589321



Internal ID16030044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1122625..2165018hg38UCSC Ensembl
Innerchr3:1164309..2206702hg19UCSC Ensembl
Innerchr3:1139309..2181702hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381042394
hg191042394
hg181042394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8157n54
Supporting Variantsnssv957825
Samples
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)nsv589321
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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