A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177795



Internal ID20744835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86464172..86464712hg38UCSC Ensembl
chr16:86497778..86498318hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505186
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.74614


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