A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461060



Internal ID239025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166495220..166496353hg38UCSC Ensembl
chr6:166908708..166909841hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990594
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461060
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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