A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901859



Internal ID2037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46329126..46329126hg38UCSC Ensembl
chr1:46794798..46794798hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5399190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901859
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008065


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