A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4717n100



Internal ID22790804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35752672..35907323hg38UCSC Ensembl
chr3:35794164..35948815hg19UCSC Ensembl
chr3:35769168..35923819hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38154652
hg19154652
hg18154652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012445, nsv1001457, nsv1004321, nsv997945, nsv997763, nsv1003566, nsv1001440, nsv1011496, nsv1010151, nsv1000571, nsv999190, nsv1009026, nsv1001307, nsv1012374, nsv1012994, nsv1004393, nsv1007758, nsv999830
Samples
Known GenesARPP21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4717n100
Frequency
Sample Size11257
Observed Gain72
Observed Loss0
Observed Complex0
Frequencyn/a


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