A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088087



Internal ID21997320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46366399..46366399hg38UCSC Ensembl
chr15:46658597..46658597hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088087
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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