A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14256909



Internal ID22295366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:45372376..45383983hg38UCSC Ensembl
Outerchr13:45946511..45958118hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3811608
hg1911608
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214612
Supporting Variants
SamplesNA19240
Known GenesTPT1-AS1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14256909
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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