A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216455



Internal ID20783495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58434576..58473460hg38UCSC Ensembl
chr5:57730403..57769287hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3838885
hg1938885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403132
Supporting Variants
Samples
Known GenesPLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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