A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202269



Internal ID20769309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4166365..4168935hg38UCSC Ensembl
chr20:4147012..4149582hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382571
hg192571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530590
Supporting Variants
Samples
Known GenesSMOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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