A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14258512



Internal ID22230841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:91404734..91459392hg38UCSC Ensembl
Outerchr15:91947964..92002622hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3854659
hg1954659
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226098
Supporting Variants
SamplesHG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14258512
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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