A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202997



Internal ID20770037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8917919..9087644hg38UCSC Ensembl
chr20:8898566..9068291hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38169726
hg19169726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524598
Supporting Variants
Samples
Known GenesPLCB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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