A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556914



Internal ID18757990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19080795..19081080hg38UCSC Ensembl
Outerchr20:19080724..19081128hg38UCSC Ensembl
Innerchr20:19061439..19061724hg19UCSC Ensembl
Outerchr20:19061368..19061772hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755661
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556914
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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