A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225352



Internal ID22368509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45155973..45156224hg38UCSC Ensembl
chr21:46575888..46576139hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301753, nssv14301752
SamplesNA19238, HG00733
Known GenesADARB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225352
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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