A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986737



Internal ID58597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108683694..108683956hg38UCSC Ensembl
chr6:109004897..109005159hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140871
Supporting Variants
Samples
Known GenesFOXO3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003124


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