A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4709n100



Internal ID22790796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26297590..26392621hg38UCSC Ensembl
chr3:26339081..26434112hg19UCSC Ensembl
chr3:26314085..26409116hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3895032
hg1995032
hg1895032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001468, nsv1000716, nsv998667
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4709n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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