A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092408



Internal ID22001641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37847757..37847757hg38UCSC Ensembl
chr9:37847754..37847754hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596383
Samples
Known GenesDCAF10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092408
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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