A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589390



Internal ID16030113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2531464..2628024hg38UCSC Ensembl
Innerchr3:2573148..2669708hg19UCSC Ensembl
Innerchr3:2548148..2644708hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3896561
hg1996561
hg1896561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8170n54
Supporting Variantsnssv957988
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589390
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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