A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792881



Internal ID19175235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26145712..26320138hg38UCSC Ensembl
Innerchr20:26126348..26300774hg19UCSC Ensembl
Innerchr20:26074348..26248774hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38174427
hg19174427
hg18174427
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893328
Supporting Variants
Samples
Known GenesLOC284801, MIR663A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792881
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer