A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896614



Internal ID22671708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133808293..133808868hg38UCSC Ensembl
chr3:133527137..133527712hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397954
Samples
Known GenesSRPRB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896614
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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