A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100266



Internal ID22009499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90020814..90020814hg38UCSC Ensembl
chr14:90487158..90487158hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616096
Samples
Known GenesTDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100266
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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