A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980890



Internal ID54630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27823804..27828731hg38UCSC Ensembl
chr6:27791582..27796509hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384928
hg194928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473492
Supporting Variants
Samples
Known GenesHIST1H4J
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980890
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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