A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787555



Internal ID18818315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55805430..55857497hg38UCSC Ensembl
Innerchr19:56316796..56368863hg19UCSC Ensembl
Innerchr19:61008608..61060675hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3852068
hg1952068
hg1852068
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893253
Supporting Variants
Samples
Known GenesNLRP11, NLRP4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=46
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787555
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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