A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839059



Internal ID22613994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:49487413..49496596hg38UCSC Ensembl
chr4:49489430..49498613hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg389184
hg199184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495288, nssv17495290, nssv17495289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839059
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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