A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896786



Internal ID22671882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141594141..141594543hg38UCSC Ensembl
chr5:140973708..140974110hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413983
Samples
Known GenesDIAPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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