A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969972



Internal ID47302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128699059..128842071hg38UCSC Ensembl
chr6:129020204..129163216hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38143013
hg19143013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969972
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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