A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893321



Internal ID19184141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23701496..23746320hg38UCSC Ensembl
Outerchr20:23691103..23752605hg38UCSC Ensembl
Innerchr20:23682133..23726957hg19UCSC Ensembl
Outerchr20:23671740..23733242hg19UCSC Ensembl
Innerchr20:23630133..23674957hg18UCSC Ensembl
Outerchr20:23619740..23681242hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3861503
hg1961503
hg1861503
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780182, essv25788384, essv25789509
Samples
Known GenesCST1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893321
Frequency
Sample Size3017
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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