A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894149



Internal ID19185218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18777529..18823532hg38UCSC Ensembl
Outerchr5:18777529..18823532hg38UCSC Ensembl
Innerchr5:18777638..18823641hg19UCSC Ensembl
Outerchr5:18777638..18823641hg19UCSC Ensembl
Innerchr5:18813395..18859398hg18UCSC Ensembl
Outerchr5:18813395..18859398hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3846004
hg1946004
hg1846004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797611
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894149
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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