A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901279



Internal ID1666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31489835..31506000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3816166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429422
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901279
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000158


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