A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222092



Internal ID22366277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134172951..134181050hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9787n152
Supporting Variantsnssv14347879, nssv14347885, nssv14347884, nssv14347886, nssv14347881, nssv14347880, nssv14347882, nssv14347883, nssv14347887
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222092
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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