A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14258413



Internal ID22278399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:97981784..97998861hg38UCSC Ensembl
Outerchr15:98525014..98542091hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3817078
hg1917078
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225230
Supporting Variants
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14258413
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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