A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589382



Internal ID16030105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2454047..2454612hg38UCSC Ensembl
Innerchr3:2495731..2496296hg19UCSC Ensembl
Innerchr3:2470731..2471296hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38566
hg19566
hg18566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8168n54
Supporting Variantsnssv957920
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589382
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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