A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991144



Internal ID61504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161567720..162085660hg38UCSC Ensembl
chr6:161988752..162506692hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38517941
hg19517941
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462490
Supporting Variants
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991144
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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