A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14302634



Internal ID22284495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10940790..10945005hg38UCSC Ensembl
chrUn_gl000241:16218..20433hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384216
hg194216
Variant TypeCNV duplication
Copy Number6
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220897
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14302634
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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