A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835688



Internal ID22610623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179670641..179672240hg38UCSC Ensembl
chr3:179388429..179390028hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489727
Samples
Known GenesUSP13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835688
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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