A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981029



Internal ID54729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14133803..14133838hg38UCSC Ensembl
chr6:14134034..14134069hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538636
Supporting Variants
Samples
Known GenesCD83
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981029
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.020657


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