A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933381



Internal ID22708693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99302836..99302893hg38UCSC Ensembl
chr13:99955090..99955147hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374724
Samples
Known GenesGPR183, MIR548AN, UBAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933381
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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