A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046794



Internal ID21956027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40618184..40618264hg38UCSC Ensembl
chr22:41014188..41014268hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643337
Samples
Known GenesMKL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046794
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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