A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906970



Internal ID5430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94917190..94917306hg38UCSC Ensembl
chr1:95382746..95382862hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424485
Supporting Variants
Samples
Known GenesCNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906970
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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