A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009279



Internal ID18751810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2170540..2493088hg38UCSC Ensembl
Innerchr3:2212224..2534772hg19UCSC Ensembl
Innerchr3:2187224..2509772hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38322549
hg19322549
hg18322549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590367
Samples
Known GenesCNTN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009279
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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