A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263018



Internal ID20830058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128821498..128822452hg38UCSC Ensembl
chr4:129742653..129743607hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561239
Supporting Variants
Samples
Known GenesJADE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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