A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024287



Internal ID21933630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66559898..66562199hg38UCSC Ensembl
chr15:66852236..66854537hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604725
Samples
Known GenesLCTL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024287
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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