A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566978



Internal ID21515309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166416041..166416093hg38UCSC Ensembl
chr6:166829529..166829581hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158966
SamplesHG01596
Known GenesRPS6KA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566978
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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