A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211053



Internal ID20778093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13357466..13381694hg38UCSC Ensembl
chr4:13359090..13383318hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3824229
hg1924229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372171
Supporting Variants
Samples
Known GenesRAB28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211053
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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