A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222428



Internal ID22366505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33985339..33985398hg38UCSC Ensembl
chr21:35357640..35357699hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301912, nssv14301911
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222428
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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