A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456718



Internal ID234779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169255096..169302781hg38UCSC Ensembl
chr6:169655191..169702876hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3847686
hg1947686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456718
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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