A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214952



Internal ID20781992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86249201..86273100hg38UCSC Ensembl
chr5:85545019..85568918hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3823900
hg1923900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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