A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990987



Internal ID61404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166247564..166248969hg38UCSC Ensembl
chr6:166661052..166662457hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990987
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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