A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792453



Internal ID18831864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20605819..20831597hg38UCSC Ensembl
Innerchr19:20788625..21014403hg19UCSC Ensembl
Innerchr19:20580465..20806243hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38225779
hg19225779
hg18225779
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893177
Supporting Variants
Samples
Known GenesZNF626
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=54
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792453
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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