A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14366109



Internal ID22202963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73120260..73120348hg38UCSC Ensembl
chr13:73694397..73694485hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeOTHER complex substitution
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525420
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14366109
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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