A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986363



Internal ID58339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109165470..109165544hg38UCSC Ensembl
chr6:109486673..109486747hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462788
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986363
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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