A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361325



Internal ID22253008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118421954..118423117hg38UCSC Ensembl
chr11:118292669..118293832hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528721
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361325
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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