A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541343



Internal ID315962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30309882..30309895hg38UCSC Ensembl
chr8:30167398..30167411hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541343
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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