A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988622



Internal ID59839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105316063..105316114hg38UCSC Ensembl
chr6:105763938..105763989hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412160
Supporting Variants
Samples
Known GenesPREP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988622
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001873


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