A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14302123



Internal ID22279952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12132504..12162928hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3830425
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206434
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14302123
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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