A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188684



Internal ID20755724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58843701..58849800hg38UCSC Ensembl
chr16:58877605..58883704hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer