A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979465



Internal ID53691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9353298..9353506hg38UCSC Ensembl
chr6:9353531..9353739hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979465
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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