A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093627



Internal ID22002860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73491256..73491256hg38UCSC Ensembl
chr15:73783597..73783597hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606248
Samples
Known GenesC15orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093627
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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