A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214666



Internal ID22361254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45293798..45294699hg38UCSC Ensembl
chr13:45867933..45868834hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367597
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214666
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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