A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4774n100



Internal ID22790861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75355012..75500783hg38UCSC Ensembl
chr3:75404163..75549934hg19UCSC Ensembl
chr3:75486853..75632624hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38145772
hg19145772
hg18145772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011219, nsv1010072, nsv1003260, nsv1011116, nsv1001183, nsv1008271, nsv1002337, nsv1002149, nsv1003073, nsv1001084, nsv1007785, nsv1014979, nsv1009357, nsv1008082, nsv1004178, nsv1001606, nsv1013681, nsv999165, nsv1012954, nsv1014754, nsv1009223, nsv1002142, nsv998523, nsv1004717, nsv998190, nsv1006668, nsv1000051, nsv1012937, nsv1005864, nsv1012091, nsv1002352, nsv999213, nsv1013683
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)dgv4774n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss284
Observed Complex0
Frequencyn/a


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