A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225396



Internal ID22368536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8391872..8392312hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301304, nssv14301305, nssv14301301, nssv14301307, nssv14301303, nssv14301300, nssv14301306, nssv14301308, nssv14301302
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)nsv3225396
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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