A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14302128



Internal ID22186933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12162929..12177811hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3814883
Variant TypeCNV duplication
Copy Number315
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216759
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14302128
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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