A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204114



Internal ID20771154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43698857..43738766hg38UCSC Ensembl
chr21:45118738..45158647hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3839910
hg1939910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546221
Supporting Variants
Samples
Known GenesPDXK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204114
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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