A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704249



Internal ID127915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65116568..65116677hg38UCSC Ensembl
chr15:65408906..65409015hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552192
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704249
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004839


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