A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843143



Internal ID22618078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6455042..6458241hg38UCSC Ensembl
chr5:6455155..6458354hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498050
Samples
Known GenesUBE2QL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843143
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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