A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459169



Internal ID237186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146294261..146294318hg38UCSC Ensembl
chr6:146615397..146615454hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989586
Samples
Known GenesGRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459169
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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