A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14368079



Internal ID22274598
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214989
Supporting Variants
SamplesNA19239
Known GenesSTARD13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14368079
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