A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540804



Internal ID20914093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46913159..46960696hg38UCSC Ensembl
chr22:47309055..47356592hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3847538
hg1947538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075008
Samples
Known GenesTBC1D22A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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