A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990223



Internal ID60880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161931281..162475923hg38UCSC Ensembl
chr6:162352313..162896955hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38544643
hg19544643
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558452
Supporting Variants
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990223
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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