A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4856n100



Internal ID20156472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128647883..128702740hg38UCSC Ensembl
chr3:128366726..128421583hg19UCSC Ensembl
chr3:129849416..129904273hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3854858
hg1954858
hg1854858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010717, nsv1010302, nsv1013298
Samples
Known GenesRPN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4856n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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