A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025125



Internal ID21934468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46835434..46838129hg38UCSC Ensembl
chr11:46856985..46859680hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382696
hg192696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581803
Samples
Known GenesCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025125
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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