A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025817



Internal ID21935160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52084728..52084780hg38UCSC Ensembl
chr13:52658864..52658916hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612093
Samples
Known GenesNEK5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025817
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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