A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987403



Internal ID59043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79276305..79276933hg38UCSC Ensembl
chr6:79986022..79986650hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987403
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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