A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797396



Internal ID19177526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42868234..43052690hg38UCSC Ensembl
Innerchr19:43372386..43556842hg19UCSC Ensembl
Innerchr19:48064226..48248682hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38184457
hg19184457
hg18184457
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893210
Supporting Variants
Samples
Known GenesPSG1, PSG11, PSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797396
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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