A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755977



Internal ID18730223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55859648..55865453hg38UCSC Ensembl
Outerchr20:55859419..55865736hg38UCSC Ensembl
Innerchr20:54434704..54440509hg19UCSC Ensembl
Outerchr20:54434475..54440792hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386318
hg196318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755977
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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