A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025921



Internal ID21935264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50043286..50043339hg38UCSC Ensembl
chr18:47569656..47569709hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623610
Samples
Known GenesMYO5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025921
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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