A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890691



Internal ID19184993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103978774..104885172hg38UCSC Ensembl
Outerchr5:103978774..104885172hg38UCSC Ensembl
Innerchr5:103314475..104220873hg19UCSC Ensembl
Outerchr5:103314475..104220873hg19UCSC Ensembl
Innerchr5:103342374..104248772hg18UCSC Ensembl
Outerchr5:103342374..104248772hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg38906399
hg19906399
hg18906399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787836
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890691
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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