A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214989



Internal ID22361471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33558661..33564775hg38UCSC Ensembl
chr13:34132798..34138912hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg386115
hg196115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368079
SamplesNA19239
Known GenesSTARD13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214989
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer