A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4705n100



Internal ID22790792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25543343..25571444hg38UCSC Ensembl
chr3:25584834..25612935hg19UCSC Ensembl
chr3:25559838..25587939hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3828102
hg1928102
hg1828102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004065, nsv999523
Samples
Known GenesRARB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4705n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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