A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14405406



Internal ID22306282
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223109
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14405406
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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