A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903957



Internal ID22679130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179660074..179660131hg38UCSC Ensembl
chr3:179377862..179377919hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426673
Samples
Known GenesUSP13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903957
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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