A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097372



Internal ID22006605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26842734..26842734hg38UCSC Ensembl
chr15:27087881..27087881hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097372
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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