A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4618n100



Internal ID22790705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1029678..2002762hg38UCSC Ensembl
chr3:1071362..2044446hg19UCSC Ensembl
chr3:1046362..2019446hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38973085
hg19973085
hg18973085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997851, nsv1012550
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)dgv4618n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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