A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4711n100



Internal ID22790798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26491082..26541717hg38UCSC Ensembl
chr3:26532573..26583208hg19UCSC Ensembl
chr3:26507577..26558212hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3850636
hg1950636
hg1850636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004322, nsv1010815
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)dgv4711n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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