A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203364



Internal ID20770404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60737408..60745576hg38UCSC Ensembl
chr20:59312466..59320633hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388169
hg198168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203364
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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