A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084628



Internal ID21993861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67609444..67609444hg38UCSC Ensembl
chr15:67901782..67901782hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598524
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084628
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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