A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985461



Internal ID57714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93740953..93741039hg38UCSC Ensembl
chr6:94450671..94450757hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469440
Supporting Variants
Samples
Known GenesTSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985461
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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