A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891368



Internal ID168433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160235145..160235774hg38UCSC Ensembl
chr1:160204935..160205564hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415999
Supporting Variants
Samples
Known GenesDCAF8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891368
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00814


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