A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526119



Internal ID20899480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23679263..23810364hg38UCSC Ensembl
chr20:23659900..23791001hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38131102
hg19131102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203235
Samples
Known GenesCST1, CST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526119
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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