A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893234



Internal ID18837368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52611014..52929801hg38UCSC Ensembl
Outerchr19:52600622..52937400hg38UCSC Ensembl
Innerchr19:53114267..53433054hg19UCSC Ensembl
Outerchr19:53103875..53440653hg19UCSC Ensembl
Innerchr19:57806079..58124866hg18UCSC Ensembl
Outerchr19:57795687..58132465hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38336779
hg19336779
hg18336779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791576, essv25788969, essv25792368
Samples
Known GenesZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF816-ZNF321P, ZNF83
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893234
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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