A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211028



Internal ID22358724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9897104..9901229hg38UCSC Ensembl
chr21:10375138..10379263hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg384126
hg194126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299298, nssv14299301, nssv14299297, nssv14299295, nssv14299300, nssv14299302, nssv14299299, nssv14299303, nssv14299296
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)nsv3211028
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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