A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024443



Internal ID21933786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89376225..89376283hg38UCSC Ensembl
chr15:89919456..89919514hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024443
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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