A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837605



Internal ID22612540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121811994..121818450hg38UCSC Ensembl
chr4:122733149..122739605hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg386457
hg196457
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498324
Samples
Known GenesCCNA2, EXOSC9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837605
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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