A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789580



Internal ID19170658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53399360..53479458hg38UCSC Ensembl
Innerchr19:53902613..53982712hg19UCSC Ensembl
Innerchr19:58594425..58674524hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3880099
hg1980100
hg1880100
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893243
Supporting Variants
Samples
Known GenesTPM3P9, ZNF761, ZNF765, ZNF813
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789580
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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