A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893194



Internal ID18837328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27310906..28125100hg38UCSC Ensembl
Outerchr19:27310906..28125100hg38UCSC Ensembl
Innerchr19:27801814..28616007hg19UCSC Ensembl
Outerchr19:27801814..28616007hg19UCSC Ensembl
Innerchr19:32493654..33307847hg18UCSC Ensembl
Outerchr19:32493654..33307847hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38814195
hg19814194
hg18814194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788128
Samples
Known GenesLINC00662
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893194
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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