A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4603n100



Internal ID22790690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18655..81831hg38UCSC Ensembl
chr3:60333..123514hg19UCSC Ensembl
chr3:35333..98514hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3863177
hg1963182
hg1863182
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999171, nsv1012781
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)dgv4603n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss2
Observed Complex0
Frequencyn/a


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