A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215736



Internal ID20782776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2630542..2668067hg38UCSC Ensembl
chr5:2630656..2668181hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3837526
hg1937526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215736
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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