A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036232



Internal ID91900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59008607..59008658hg38UCSC Ensembl
chr10:60768367..60768418hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5396115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036232
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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