A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3247269



Internal ID22376662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:45374712..45384109hg38UCSC Ensembl
Outerchr13:45948847..45958244hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg388561
hg198561
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14257531, nssv14257532
SamplesNA19239, NA19240
Known GenesTPT1-AS1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3247269
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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