A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896829



Internal ID172036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226494147..226494147hg38UCSC Ensembl
chr1:226681848..226681848hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5404817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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