A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791576



Internal ID18814690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52611014..52929801hg38UCSC Ensembl
Innerchr19:53114267..53433054hg19UCSC Ensembl
Innerchr19:57806079..58124866hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38318788
hg19318788
hg18318788
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893234
Supporting Variants
Samples
Known GenesZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF816-ZNF321P, ZNF83
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=71
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791576
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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