A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083843



Internal ID21993076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128808408..128808408hg38UCSC Ensembl
chr9:131570687..131570687hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578567
Samples
Known GenesTBC1D13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083843
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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