A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050332



Internal ID21959565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32305232..32306946hg38UCSC Ensembl
chr20:30893035..30894749hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381715
hg191715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637299
Samples
Known GenesKIF3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050332
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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