A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182229



Internal ID20749269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11567194..11568062hg38UCSC Ensembl
chr16:11661050..11661918hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38869
hg19869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498022
Supporting Variants
Samples
Known GenesLITAF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182229
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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