A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090025



Internal ID21999258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25847466..25847466hg38UCSC Ensembl
chr15:26092613..26092613hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600081
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090025
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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