A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989556



Internal ID60463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145755021..145755072hg38UCSC Ensembl
chr6:146076157..146076208hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395902
Supporting Variants
Samples
Known GenesLOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989556
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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