A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702373



Internal ID126039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71182071..71185597hg38UCSC Ensembl
chr15:71474410..71477936hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383527
hg193527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530803
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702373
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.016079


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