A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908261



Internal ID6303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86358366..86358417hg38UCSC Ensembl
chr1:86824049..86824100hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412975
Supporting Variants
Samples
Known GenesODF2L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908261
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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