A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541962



Internal ID20915230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46382690..46383666hg38UCSC Ensembl
chr21:47802605..47803581hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204208
Samples
Known GenesPCNT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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