A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907789



Internal ID5975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106539177..106539713hg38UCSC Ensembl
chr1:107081799..107082335hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.011396


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