A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14366151



Internal ID22134564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74165319..74166109hg38UCSC Ensembl
chr13:74739456..74740246hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216485
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14366151
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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