A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024524



Internal ID21933867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70632431..70632541hg38UCSC Ensembl
chr15:70924770..70924880hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024524
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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