A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991371



Internal ID61658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170559000..170615393hg38UCSC Ensembl
chr6:170868088..170924481hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3856394
hg1956394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454360
Supporting Variants
Samples
Known GenesPDCD2, TBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991371
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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