A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461061



Internal ID239026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134659254..134659308hg38UCSC Ensembl
chr6:134980392..134980446hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461061
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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