A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557162



Internal ID18758238
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 StatusM
Merged Variants
Supporting Variantsessv9755909
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557162
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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