A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215745



Internal ID20782785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26756124..26775414hg38UCSC Ensembl
chr5:26756233..26775523hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3819291
hg1919291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215745
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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