A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755532



Internal ID18729778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6170312..6170628hg38UCSC Ensembl
Outerchr20:6170262..6170678hg38UCSC Ensembl
Innerchr20:6150959..6151275hg19UCSC Ensembl
Outerchr20:6150909..6151325hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755532
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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