A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142788



Internal ID341989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166783671..166783873hg38UCSC Ensembl
chr6:167197159..167197361hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991221
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142788
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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