A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089005



Internal ID21998238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70130054..70130054hg38UCSC Ensembl
chr15:70422393..70422393hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089005
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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