A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026402



Internal ID21935745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46749023..46749081hg38UCSC Ensembl
chr11:46770573..46770631hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580383
Samples
Known GenesCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026402
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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