A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455517



Internal ID233596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106085575..106085744hg38UCSC Ensembl
chr6:106533450..106533619hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455517
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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