A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902446



Internal ID2441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26239551..26239614hg38UCSC Ensembl
chr1:26566042..26566105hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431446
Supporting Variants
Samples
Known GenesCEP85
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902446
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.021549


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