A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969776



Internal ID47166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131906949..131907031hg38UCSC Ensembl
chr6:132228089..132228171hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460884
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969776
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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