A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203346



Internal ID20770386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5908201..5912700hg38UCSC Ensembl
chr20:5888847..5893346hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530825
Supporting Variants
Samples
Known GenesCHGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203346
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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