A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797844



Internal ID19175568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42897784..43191688hg38UCSC Ensembl
Innerchr19:43401936..43695840hg19UCSC Ensembl
Innerchr19:48093776..48387680hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38293905
hg19293905
hg18293905
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893216
Supporting Variants
Samples
Known GenesPSG11, PSG2, PSG5, PSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797844
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