A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735856



Internal ID159522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117564973..117565010hg38UCSC Ensembl
chr8:118577212..118577249hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735856
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004527


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