A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788610



Internal ID18819120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6556767..6641331hg38UCSC Ensembl
Innerchr19:6556778..6641342hg19UCSC Ensembl
Innerchr19:6507778..6592342hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3884565
hg1984565
hg1884565
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893161
Supporting Variants
Samples
Known GenesCD70
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788610
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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