A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893258



Internal ID18837392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57803309..57980259hg38UCSC Ensembl
Outerchr19:57803309..57980259hg38UCSC Ensembl
Innerchr19:58314677..58491627hg19UCSC Ensembl
Outerchr19:58314677..58491627hg19UCSC Ensembl
Innerchr19:63006489..63183439hg18UCSC Ensembl
Outerchr19:63006489..63183439hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38176951
hg19176951
hg18176951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788939
Samples
Known GenesC19orf18, FKBP1AP1, ZNF256, ZNF417, ZNF418, ZNF552, ZNF587, ZNF587B, ZNF606, ZNF814
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893258
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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