A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024699



Internal ID21934042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19781291..19781460hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024699
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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