A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786821



Internal ID19160355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54245159hg38UCSC Ensembl
Innerchr19:54731679..54749011hg19UCSC Ensembl
Innerchr19:59423491..59440823hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817355
hg1917333
hg1817333
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893247
Supporting Variants
Samples
Known GenesLILRA6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786821
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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