A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380686



Internal ID22326589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92767811..92769752hg38UCSC Ensembl
chr15:93311041..93312982hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381942
hg191942
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212712
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380686
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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