A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562092



Internal ID22430854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32342708..32342708hg38UCSC Ensembl
chr21:33715017..33715017hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301860, nssv14301856, nssv14301852, nssv14301858, nssv14301853, nssv14301857, nssv14301854, nssv14301859, nssv14301855
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesURB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562092
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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