A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979398



Internal ID53637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28050213..28054688hg38UCSC Ensembl
chr6:28017991..28022466hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384476
hg194476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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