A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864653



Internal ID22639588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48052473..48058172hg38UCSC Ensembl
chr8:48965033..48970732hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509260
Samples
Known GenesUBE2V2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864653
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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