A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589363



Internal ID16030086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1868843..2531777hg38UCSC Ensembl
Innerchr3:1910527..2573461hg19UCSC Ensembl
Innerchr3:1885527..2548461hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38662935
hg19662935
hg18662935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957903
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589363
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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