A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466042



Internal ID243892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110573988..110574675hg38UCSC Ensembl
chr6:110895191..110895878hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466042
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer