A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355299



Internal ID22283179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12286546..12288915hg38UCSC Ensembl
chr11:12308093..12310462hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382370
hg192370
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226536
Supporting Variants
SamplesNA19239
Known GenesMICALCL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355299
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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