A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893720



Internal ID19184540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:69482713..69533979hg38UCSC Ensembl
Outerchr3:69482713..69533979hg38UCSC Ensembl
Innerchr3:69531864..69583130hg19UCSC Ensembl
Outerchr3:69531864..69583130hg19UCSC Ensembl
Innerchr3:69614554..69665820hg18UCSC Ensembl
Outerchr3:69614554..69665820hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3851267
hg1951267
hg1851267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788488
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893720
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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