A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838745



Internal ID22613680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183988797..183994571hg38UCSC Ensembl
chr4:184909950..184915724hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg385775
hg195775
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491341
Samples
Known GenesSTOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838745
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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