A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4815n100



Internal ID22790902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95113446..95519455hg38UCSC Ensembl
chr3:94832290..95238299hg19UCSC Ensembl
chr3:96314980..96720989hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38406010
hg19406010
hg18406010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011235, nsv999347
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)dgv4815n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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