A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4908n100



Internal ID20156524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138494324..139018846hg38UCSC Ensembl
chr3:138213166..138737688hg19UCSC Ensembl
chr3:139695856..140220378hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38524523
hg19524523
hg18524523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010514, nsv1013074, nsv1009726
Samples
Known GenesC3orf72, CEP70, FAIM, FOXL2, PIK3CB, PRR23A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4908n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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