A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211332



Internal ID22358920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9916639..9920957hg38UCSC Ensembl
chr21:10394667..10398985hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg384319
hg194319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299318, nssv14299322, nssv14299321, nssv14299314, nssv14299317, nssv14299319, nssv14299320, nssv14299315, nssv14299316
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)nsv3211332
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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