A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796742



Internal ID19179434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42886210..42964507hg38UCSC Ensembl
Innerchr19:43390362..43468659hg19UCSC Ensembl
Innerchr19:48082202..48160499hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3878298
hg1978298
hg1878298
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893214
Supporting Variants
Samples
Known GenesPSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796742
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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