A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798808



Internal ID19178736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43057570..43089269hg38UCSC Ensembl
Innerchr19:43561722..43593421hg19UCSC Ensembl
Innerchr19:48253562..48285261hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3831700
hg1931700
hg1831700
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893212
Supporting Variants
Samples
Known GenesPSG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798808
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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