A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979421



Internal ID53658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5931082..5969170hg38UCSC Ensembl
chr6:5931315..5969403hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3838089
hg1938089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471685
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979421
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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