A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350238



Internal ID22277390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138279608..138282592hg38UCSC Ensembl
chr11:125086..128088hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382985
hg193003
Variant TypeCNV duplication
Copy Number36
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229819
Supporting Variants
SamplesNA19239
Known GenesLINC01001
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350238
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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