A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787173



Internal ID19179608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20164128..20172285hg38UCSC Ensembl
Innerchr20:20144772..20152929hg19UCSC Ensembl
Innerchr20:20092772..20100929hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg388158
hg198158
hg188158
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893320
Supporting Variants
Samples
Known GenesC20orf26
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787173
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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