A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084451



Internal ID21993684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60913123..60913123hg38UCSC Ensembl
chr15:61205322..61205322hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg382890
hg192890
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599557
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084451
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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