A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797764



Internal ID19182144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42867142..43076596hg38UCSC Ensembl
Innerchr19:43371294..43580748hg19UCSC Ensembl
Innerchr19:48063134..48272588hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38209455
hg19209455
hg18209455
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893210
Supporting Variants
Samples
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797764
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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