A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185100



Internal ID20752140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4153654..4162166hg38UCSC Ensembl
chr16:4203655..4212167hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388513
hg198513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185100
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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