A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893243



Internal ID19184063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53407265..53472214hg38UCSC Ensembl
Outerchr19:53399360..53479458hg38UCSC Ensembl
Innerchr19:53910518..53975468hg19UCSC Ensembl
Outerchr19:53902613..53982712hg19UCSC Ensembl
Innerchr19:58602330..58667280hg18UCSC Ensembl
Outerchr19:58594425..58674524hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3880099
hg1980100
hg1880100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788230, essv25789580
Samples
Known GenesTPM3P9, ZNF761, ZNF765, ZNF813
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893243
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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