A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213525



Internal ID22360446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66146688..66147036hg38UCSC Ensembl
chr13:66720820..66721168hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2313n152
Supporting Variantsnssv14369072, nssv14369071, nssv14369073
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213525
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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