A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187718



Internal ID20754758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87391601..87394300hg38UCSC Ensembl
chr16:87425207..87427906hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504059
Supporting Variants
Samples
Known GenesFBXO31, MAP1LC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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