A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988990



Internal ID60083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149554797..149564776hg38UCSC Ensembl
chr6:149875933..149885912hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg389980
hg199980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988990
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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