A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097343



Internal ID22006576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46830909..46830909hg38UCSC Ensembl
chr11:46852460..46852460hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382271
hg192271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581682
Samples
Known GenesCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097343
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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