A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704453



Internal ID128119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80481990..80482026hg38UCSC Ensembl
chr15:80774331..80774367hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551827
Supporting Variants
Samples
Known GenesARNT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704453
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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