A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14366114



Internal ID22202965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73162298..73162810hg38UCSC Ensembl
chr13:73736435..73736947hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236327
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14366114
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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