A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906595



Internal ID5180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101842693..101842908hg38UCSC Ensembl
chr1:102308249..102308464hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424566
Supporting Variants
Samples
Known GenesOLFM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906595
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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