A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048776



Internal ID21958011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40470964..40483418hg38UCSC Ensembl
chr22:40866968..40879422hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3812455
hg1912455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644834
Samples
Known GenesMKL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048776
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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