A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14302096



Internal ID22273419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11960245..11962563hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382319
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199910
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14302096
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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