A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093791



Internal ID22003024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121959040..121959040hg38UCSC Ensembl
chr10:123718555..123718555hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580406
Samples
Known GenesNSMCE4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093791
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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