A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986926



Internal ID58732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92933460..92963736hg38UCSC Ensembl
chr6:93643178..93673454hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3830277
hg1930277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467757
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986926
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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