A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081016



Internal ID21990249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97014971..97014971hg38UCSC Ensembl
chr15:97558201..97558201hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385964
hg195964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081016
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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