A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014279



Internal ID21923622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115930434..115930519hg38UCSC Ensembl
chr5:115266131..115266216hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014279
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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