A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589375



Internal ID16030098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2312351..2910530hg38UCSC Ensembl
Innerchr3:2354035..2952214hg19UCSC Ensembl
Innerchr3:2329035..2927214hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38598180
hg19598180
hg18598180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8165n54
Supporting Variantsnssv957909, nssv1152442
Samples1780854080_A
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589375
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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