A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005841



Internal ID21915184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138143607..138143673hg38UCSC Ensembl
chr5:137479296..137479362hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543658
Samples
Known GenesBRD8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005841
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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