A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212915



Internal ID20779955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:341355..566560hg38UCSC Ensembl
chr4:335144..560349hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38225206
hg19225206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373163
Supporting Variants
Samples
Known GenesABCA11P, PIGG, ZNF141, ZNF721
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212915
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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