A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022227



Internal ID21931570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111340484..111340545hg38UCSC Ensembl
chr13:111992831..111992892hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609110
Samples
Known GenesTEX29
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022227
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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