A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4778n100



Internal ID22790865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75372007..75620267hg38UCSC Ensembl
chr3:75421158..75669418hg19UCSC Ensembl
chr3:75503848..75752108hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38248261
hg19248261
hg18248261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007400, nsv997567, nsv1004331
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4778n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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