A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796938



Internal ID19169372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42886210..43009507hg38UCSC Ensembl
Innerchr19:43390362..43513659hg19UCSC Ensembl
Innerchr19:48082202..48205499hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38123298
hg19123298
hg18123298
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893210
Supporting Variants
Samples
Known GenesPSG11, PSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796938
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer