A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017903



Internal ID79588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115753415..115753466hg38UCSC Ensembl
chr8:116765641..116765692hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5401774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017903
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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