A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893158



Internal ID18837292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4856682..4900672hg38UCSC Ensembl
Outerchr19:4856682..4900672hg38UCSC Ensembl
Innerchr19:4856694..4900684hg19UCSC Ensembl
Outerchr19:4856694..4900684hg19UCSC Ensembl
Innerchr19:4807694..4851684hg18UCSC Ensembl
Outerchr19:4807694..4851684hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3843991
hg1943991
hg1843991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786373
Samples
Known GenesARRDC5, PLIN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893158
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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