A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991338



Internal ID61636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170368995..170369127hg38UCSC Ensembl
chr6:170678083..170678215hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463852
Supporting Variants
Samples
Known GenesFAM120B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991338
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.030284


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