A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982465



Internal ID55668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29437545..29437545hg38UCSC Ensembl
chr6:29405322..29405322hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982465
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.050502


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