A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986388



Internal ID58358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109468833..109468891hg38UCSC Ensembl
chr6:109790036..109790094hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467894
Supporting Variants
Samples
Known GenesZBTB24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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