A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215862



Internal ID20782902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132786772..132809457hg38UCSC Ensembl
chr5:132122464..132145149hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3822686
hg1922686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405998
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215862
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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