A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755982



Internal ID18730228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56188986..56189153hg38UCSC Ensembl
Outerchr20:56188967..56189178hg38UCSC Ensembl
Innerchr20:54764042..54764209hg19UCSC Ensembl
Outerchr20:54764023..54764234hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755982
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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