A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561129



Internal ID21885484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166640304..166640304hg38UCSC Ensembl
chr6:167053792..167053792hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381367
hg191367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079587
Supporting Variants
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561129
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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