A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5471653



Internal ID249383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166736173..166736331hg38UCSC Ensembl
chr6:167149661..167149819hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991216
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5471653
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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