A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701935



Internal ID125601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35905652..35905703hg38UCSC Ensembl
chr15:36197853..36197904hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701935
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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