A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715602



Internal ID139268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81683637..81683674hg38UCSC Ensembl
chr17:79650667..79650704hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536199
Supporting Variants
Samples
Known GenesARL16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715602
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.013425


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