A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299331



Internal ID22322665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9943772..9953830hg38UCSC Ensembl
chr21:10421800..10431858hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3810059
hg1910059
Variant TypeCNV duplication
Copy Number7
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224668
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299331
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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