A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099037



Internal ID22008270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70541071..70541071hg38UCSC Ensembl
chr15:70833410..70833410hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099037
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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