A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089040



Internal ID21998273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75626595..75626595hg38UCSC Ensembl
chr13:76200731..76200731hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611373
Samples
Known GenesLMO7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089040
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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