A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038246



Internal ID21947589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69832341..69832399hg38UCSC Ensembl
chr15:70124680..70124738hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038246
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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