A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091835



Internal ID22001068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43146447..43146447hg38UCSC Ensembl
chr2:114229233..114229233hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577862
Samples
Known GenesCBWD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091835
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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