A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025094



Internal ID21934437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125432585..125434638hg38UCSC Ensembl
chr11:125302481..125304534hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604159
Samples
Known GenesPKNOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025094
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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