A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225791



Internal ID22368814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87210391..87210724hg38UCSC Ensembl
chr9:89825306..89825639hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9642n152
Supporting Variantsnssv14348101, nssv14348102, nssv14348100, nssv14348099, nssv14348097, nssv14348098
SamplesHG00512, NA19238, NA19239, HG00731, NA19240, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225791
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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