A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4790n100



Internal ID22790877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75458231..75777023hg38UCSC Ensembl
chr3:75507382..75826174hg19UCSC Ensembl
chr3:75590072..75908864hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38318793
hg19318793
hg18318793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002847, nsv1001801, nsv1011756, nsv999192, nsv1010147, nsv1013154, nsv1012775, nsv1008502, nsv1001674, nsv1012001, nsv1009064
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4790n100
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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