A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905063



Internal ID22680244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31677786..31678105hg38UCSC Ensembl
chr3:31719278..31719597hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427879
Samples
Known GenesOSBPL10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905063
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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