A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788128



Internal ID18828653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27310906..28125100hg38UCSC Ensembl
Innerchr19:27801814..28616007hg19UCSC Ensembl
Innerchr19:32493654..33307847hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38814195
hg19814194
hg18814194
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893194
Supporting Variants
Samples
Known GenesLINC00662
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=85
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788128
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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