A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205023



Internal ID20772063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31855511..31915680hg38UCSC Ensembl
chr22:32251497..32311666hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3860170
hg1960170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548879
Supporting Variants
Samples
Known GenesDEPDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205023
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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