A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022421



Internal ID21931764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52136555..52137288hg38UCSC Ensembl
chr13:52710691..52711424hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614860
Samples
Known GenesNEK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022421
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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