A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210313



Internal ID20777353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128809401..128813400hg38UCSC Ensembl
chr4:129730556..129734555hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378590
Supporting Variants
Samples
Known GenesJADE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210313
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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