A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012437



Internal ID75968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58626887..58626938hg38UCSC Ensembl
chr8:59539446..59539497hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406381
Supporting Variants
Samples
Known GenesNSMAF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012437
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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