A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360136



Internal ID22197299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95485513..95486717hg38UCSC Ensembl
chr11:95218677..95219881hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219487
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360136
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