A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099818



Internal ID22009051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74910712..74910712hg38UCSC Ensembl
chr15:75203053..75203053hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099818
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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