A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989179



Internal ID60212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159479610..159479618hg38UCSC Ensembl
chr6:159900642..159900650hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989179
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.27443


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