A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203235



Internal ID20770275
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 StatusS
Merged Variantsnsv6526119
Supporting Variants
Samples
Known GenesCST1, CST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203235
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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