A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144264



Internal ID21499379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166838746..166838922hg38UCSC Ensembl
chr6:167252234..167252410hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576667
Supporting Variants
SamplesNA19239
Known GenesRPS6KA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144264
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