A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189150



Internal ID20756190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59948998..60028556hg38UCSC Ensembl
chr16:59982902..60062460hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3879559
hg1979559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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