A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702101



Internal ID125767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77029633..77076967hg38UCSC Ensembl
chr15:77321974..77369309hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3847335
hg1947336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514962
Supporting Variants
Samples
Known GenesPSTPIP1, TSPAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702101
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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