A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553211



Internal ID20926320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43281001..43283000hg38UCSC Ensembl
chr21:44700881..44702880hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553211
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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