A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022499



Internal ID21931842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53417886..53421843hg38UCSC Ensembl
chr15:53710083..53714040hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383958
hg193958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022499
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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