A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983381



Internal ID56296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57159935..57160013hg38UCSC Ensembl
chr6:57024733..57024811hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463295
Supporting Variants
Samples
Known GenesZNF451
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983381
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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