A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755909



Internal ID18730155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:50156258..50156510hg38UCSC Ensembl
Outerchr20:50156221..50156577hg38UCSC Ensembl
Innerchr20:48772795..48773047hg19UCSC Ensembl
Outerchr20:48772758..48773114hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755909
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