A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4636n100



Internal ID20156252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2825734..3271845hg38UCSC Ensembl
chr3:2867418..3313529hg19UCSC Ensembl
chr3:2842418..3288529hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38446112
hg19446112
hg18446112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002716, nsv1004590, nsv997550
Samples
Known GenesCNTN4, CRBN, IL5RA, TRNT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4636n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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