A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087748



Internal ID21996981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66624934..66624934hg38UCSC Ensembl
chr15:66917272..66917272hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087748
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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