A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784961



Internal ID19173310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42843934..42979717hg38UCSC Ensembl
Innerchr19:43348086..43483869hg19UCSC Ensembl
Innerchr19:48039926..48175709hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38135784
hg19135784
hg18135784
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893214
Supporting Variants
Samples
Known GenesPSG1, PSG10P, PSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784961
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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