A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705110



Internal ID128776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90252190..90302122hg38UCSC Ensembl
chr15:90795422..90845354hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3849933
hg1949933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526710
Supporting Variants
Samples
Known GenesCIB1, NGRN, TTLL13
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705110
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer