A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215722



Internal ID20782762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25484201..25503000hg38UCSC Ensembl
chr5:25484310..25503109hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3818800
hg1918800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381811
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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