A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893247



Internal ID19184067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54245159hg38UCSC Ensembl
Outerchr19:54227805..54245159hg38UCSC Ensembl
Innerchr19:54731679..54749011hg19UCSC Ensembl
Outerchr19:54731679..54749011hg19UCSC Ensembl
Innerchr19:59423491..59440823hg18UCSC Ensembl
Outerchr19:59423491..59440823hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817355
hg1917333
hg1817333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786807, essv25786496, essv25786821
Samples
Known GenesLILRA6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893247
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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