A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178843



Internal ID20745883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22316801..22320200hg38UCSC Ensembl
chr10:22605730..22609129hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443590
Supporting Variants
Samples
Known GenesCOMMD3, COMMD3-BMI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178843
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00199


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