A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024489



Internal ID21933832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84744897..84745022hg38UCSC Ensembl
chr15:85288128..85288253hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024489
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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