A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213787



Internal ID20780827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164888666..165010369hg38UCSC Ensembl
chr4:165809818..165931521hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38121704
hg19121704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376514
Supporting Variants
Samples
Known GenesFAM218A, LOC100506013, TRIM61
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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