A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213858



Internal ID20780898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168878501..168881300hg38UCSC Ensembl
chr4:169799652..169802451hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378620
Supporting Variants
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00104


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