A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219611



Internal ID22364583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8985708..8988749hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299173, nssv14299174
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219611
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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