A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215979



Internal ID20783019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16533122..16538788hg38UCSC Ensembl
chr5:16533231..16538897hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385667
hg195667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388910
Supporting Variants
Samples
Known GenesFAM134B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215979
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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