A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702379



Internal ID126045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71332325..71378537hg38UCSC Ensembl
chr15:71624664..71670876hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3846213
hg1946213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530908
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702379
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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