A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904105



Internal ID22679279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26675207..26675256hg38UCSC Ensembl
chr3:26716698..26716747hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411664
Samples
Known GenesLRRC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904105
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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