A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703748



Internal ID127414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93322000..93328066hg38UCSC Ensembl
chr15:93865229..93871295hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386067
hg196067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703748
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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