A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4623n100



Internal ID20156239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1373511..1813512hg38UCSC Ensembl
chr3:1415195..1855196hg19UCSC Ensembl
chr3:1390195..1830196hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38440002
hg19440002
hg18440002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004170, nsv1006670
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4623n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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