A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202902



Internal ID20769942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45914165..45917033hg38UCSC Ensembl
chr20:44542804..44545672hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382869
hg192869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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