A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469841



Internal ID247618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161703250..162192579hg38UCSC Ensembl
chr6:162124282..162613611hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38489330
hg19489330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991152
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469841
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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