A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4613n100



Internal ID20156229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52474..1799230hg38UCSC Ensembl
chr3:94157..1840914hg19UCSC Ensembl
chr3:69157..1815914hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381746757
hg191746758
hg181746758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999316, nsv1007015
Samples
Known GenesCHL1, CNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4613n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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