A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099342



Internal ID22008575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64692166..64692166hg38UCSC Ensembl
chr15:64984365..64984365hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615095
Samples
Known GenesOAZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099342
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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