A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988701



Internal ID59893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110070868..110071025hg38UCSC Ensembl
chr6:110392071..110392228hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473146
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988701
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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