A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202239



Internal ID20769279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38362100..38394726hg38UCSC Ensembl
chr20:36990754..37023368hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3832627
hg1932615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519999
Supporting Variants
Samples
Known GenesLBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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