A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786373



Internal ID18823855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4856682..4900672hg38UCSC Ensembl
Innerchr19:4856694..4900684hg19UCSC Ensembl
Innerchr19:4807694..4851684hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3843991
hg1943991
hg1843991
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893158
Supporting Variants
Samples
Known GenesARRDC5, PLIN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786373
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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