A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837886



Internal ID22612821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125561742..125567579hg38UCSC Ensembl
chr4:126482897..126488734hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg385838
hg195838
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1593n209
Supporting Variantsnssv17498885, nssv17492836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837886
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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