A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980702



Internal ID54513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17053263..17053357hg38UCSC Ensembl
chr6:17053494..17053588hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980702
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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