A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460574



Internal ID238553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160258136..160313285hg38UCSC Ensembl
chr6:160679168..160734317hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3855150
hg1955150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990821
Samples
Known GenesSLC22A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460574
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