A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088058



Internal ID21997291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58882181..58882181hg38UCSC Ensembl
chr15:59174380..59174380hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605841
Samples
Known GenesSLTM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088058
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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