A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893161



Internal ID18837295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6556767..6641331hg38UCSC Ensembl
Outerchr19:6556767..6641331hg38UCSC Ensembl
Innerchr19:6556778..6641342hg19UCSC Ensembl
Outerchr19:6556778..6641342hg19UCSC Ensembl
Innerchr19:6507778..6592342hg18UCSC Ensembl
Outerchr19:6507778..6592342hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3884565
hg1984565
hg1884565
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788610
Samples
Known GenesCD70
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893161
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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