A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843602



Internal ID22618537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98774921..98776520hg38UCSC Ensembl
chr5:98110625..98112224hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500160
Samples
Known GenesRGMB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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