A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536908



Internal ID312314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166930620..166930642hg38UCSC Ensembl
chr6:167344108..167344130hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991242
Samples
Known GenesRNASET2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536908
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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