A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202266



Internal ID20769306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41174634..41230328hg38UCSC Ensembl
chr20:39803274..39858968hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3855695
hg1955695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541024
Supporting Variants
Samples
Known GenesPLCG1, ZHX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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