A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4805n100



Internal ID22790892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89334971..89376652hg38UCSC Ensembl
chr3:89384121..89425802hg19UCSC Ensembl
chr3:89466811..89508492hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3841682
hg1941682
hg1841682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007183, nsv1006351, nsv1002312, nsv998808, nsv1013406, nsv1008293, nsv1014091, nsv1007800, nsv998705
Samples
Known GenesEPHA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4805n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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