A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988654



Internal ID59858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105886076..105886182hg38UCSC Ensembl
chr6:106333951..106334057hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988654
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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