A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084026



Internal ID21993259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87571515..87571515hg38UCSC Ensembl
chr9:90186430..90186430hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578824
Samples
Known GenesDAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084026
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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