A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781809



Internal ID19172586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42843934..43191688hg38UCSC Ensembl
Innerchr19:43348086..43695840hg19UCSC Ensembl
Innerchr19:48039926..48387680hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38347755
hg19347755
hg18347755
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893216
Supporting Variants
Samples
Known GenesPSG1, PSG10P, PSG11, PSG2, PSG5, PSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=49
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781809
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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