A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410794



Internal ID22468664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166709330..166709330hg38UCSC Ensembl
chr6:167122818..167122818hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952541
Supporting Variants
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410794
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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