A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013413



Internal ID21922756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170750889..170752027hg38UCSC Ensembl
chr5:170177893..170179031hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381139
hg191139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013413
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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