A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984073



Internal ID56758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69496130..69516261hg38UCSC Ensembl
chr6:70206022..70226153hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3820132
hg1920132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984073
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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