A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702160



Internal ID125826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77924606..78018356hg38UCSC Ensembl
chr15:78216948..78310698hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3893751
hg1993751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523009
Supporting Variants
Samples
Known GenesLOC645752, LOC91450, TBC1D2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702160
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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