A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755766



Internal ID18730012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34528047..34528333hg38UCSC Ensembl
Outerchr20:34527946..34528409hg38UCSC Ensembl
Innerchr20:33115852..33116138hg19UCSC Ensembl
Outerchr20:33115751..33116214hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557019
Supporting Variants
Samples
Known GenesDYNLRB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755766
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