A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093873



Internal ID22003106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80912028..80912028hg38UCSC Ensembl
chr15:81204369..81204369hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604579
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093873
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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