A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14366953



Internal ID22121642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79822866..79840014hg38UCSC Ensembl
chr13:80397001..80414149hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3817149
hg1917149
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231414
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14366953
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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