A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900537



Internal ID22675680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33428116..33439577hg38UCSC Ensembl
chr3:33469608..33481069hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3811462
hg1911462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421325
Samples
Known GenesUBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900537
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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