A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834332



Internal ID22609267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138534167..138535266hg38UCSC Ensembl
chr3:138253009..138254108hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485161, nssv17485160
Samples
Known GenesCEP70
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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