A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589393



Internal ID16030116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2920170..2920912hg38UCSC Ensembl
Innerchr3:2961854..2962596hg19UCSC Ensembl
Innerchr3:2936854..2937596hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38743
hg19743
hg18743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957991
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589393
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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