A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094777



Internal ID22004010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107388993..107388993hg38UCSC Ensembl
chr9:110151274..110151274hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094777
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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