A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571521



Internal ID21763564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166481862..166481862hg38UCSC Ensembl
chr6:166895350..166895350hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061872
Supporting Variants
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571521
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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