A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541988



Internal ID20915256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31594142..31610862hg38UCSC Ensembl
chr21:32966455..32983175hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3816721
hg1916721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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