A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182588



Internal ID20749628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1513285..1514150hg38UCSC Ensembl
chr16:1563286..1564151hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514726
Supporting Variants
Samples
Known GenesIFT140
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182588
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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