A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989531



Internal ID60445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158892700..158897617hg38UCSC Ensembl
chr6:159313732..159318649hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384918
hg194918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464459
Supporting Variants
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989531
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.005464


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