A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589368



Internal ID16030091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2053858..2744818hg38UCSC Ensembl
Innerchr3:2095542..2786502hg19UCSC Ensembl
Innerchr3:2070542..2761502hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38690961
hg19690961
hg18690961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152438
SamplesNINDS_129
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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