A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893253



Internal ID18837387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55805430..55857497hg38UCSC Ensembl
Outerchr19:55805430..55857497hg38UCSC Ensembl
Innerchr19:56316796..56368863hg19UCSC Ensembl
Outerchr19:56316796..56368863hg19UCSC Ensembl
Innerchr19:61008608..61060675hg18UCSC Ensembl
Outerchr19:61008608..61060675hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3852068
hg1952068
hg1852068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787555
Samples
Known GenesNLRP11, NLRP4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893253
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer