A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211788



Internal ID20778828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2475745..2705928hg38UCSC Ensembl
chr4:2477472..2707655hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38230184
hg19230184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360701
Supporting Variants
Samples
Known GenesFAM193A, RNF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211788
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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