A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215136



Internal ID20782176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180390385..180451127hg38UCSC Ensembl
chr5:179817385..179878127hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3860743
hg1960743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411933
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215136
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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