A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589369



Internal ID16030092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2108716..2933889hg38UCSC Ensembl
Innerchr3:2150400..2975573hg19UCSC Ensembl
Innerchr3:2125400..2950573hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38825174
hg19825174
hg18825174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8165n54
Supporting Variantsnssv1152439
SamplesNINDS_227
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589369
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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