A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979276



Internal ID53559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19865086..19867273hg38UCSC Ensembl
chr6:19865317..19867504hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382188
hg192188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979276
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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