A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989530



Internal ID60444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158891966..158893449hg38UCSC Ensembl
chr6:159312998..159314481hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381484
hg191484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460630
Supporting Variants
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989530
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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