A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893213



Internal ID19184033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43076596..43137784hg38UCSC Ensembl
Outerchr19:43039564..43191688hg38UCSC Ensembl
Innerchr19:43580748..43641936hg19UCSC Ensembl
Outerchr19:43543716..43695840hg19UCSC Ensembl
Innerchr19:48272588..48333776hg18UCSC Ensembl
Outerchr19:48235556..48387680hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38152125
hg19152125
hg18152125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787907, essv25788760, essv25788073, essv25788354, essv25788804, essv25788674, essv25787896, essv25788361, essv25791850, essv25792796, essv25789064
Samples
Known GenesPSG2, PSG5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893213
Frequency
Sample Size3017
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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