A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799792



Internal ID19162227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42868234..42961664hg38UCSC Ensembl
Innerchr19:43372386..43465816hg19UCSC Ensembl
Innerchr19:48064226..48157656hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3893431
hg1993431
hg1893431
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893214
Supporting Variants
Samples
Known GenesPSG1, PSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799792
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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