A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589384



Internal ID16030107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2454047..2454809hg38UCSC Ensembl
Innerchr3:2495731..2496493hg19UCSC Ensembl
Innerchr3:2470731..2471493hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38763
hg19763
hg18763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8168n54
Supporting Variantsnssv957979, nssv957980, nssv957977, nssv957978
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589384
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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