A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461083



Internal ID239046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159700382..159703088hg38UCSC Ensembl
chr6:160121414..160124120hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382707
hg192707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461083
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