A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562118



Internal ID22430878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37591728..37591728hg38UCSC Ensembl
chr21:38964030..38964030hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301986
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562118
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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