A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839866



Internal ID22614801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:90125644..90132100hg38UCSC Ensembl
chr4:91046795..91053251hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg386457
hg196457
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491135
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839866
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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