A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999741



Internal ID21909084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43511331..43511394hg38UCSC Ensembl
chr5:43511433..43511496hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539336
Samples
Known GenesC5orf34
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999741
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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