A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4781n100



Internal ID22790868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75400451..75466940hg38UCSC Ensembl
chr3:75449602..75516091hg19UCSC Ensembl
chr3:75532292..75598781hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3866490
hg1966490
hg1866490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006919, nsv999439, nsv1004218, nsv1014954
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)dgv4781n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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