A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027024



Internal ID21936367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6948751..6972927hg38UCSC Ensembl
chr11:6969982..6994158hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824177
hg1924177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594780
Samples
Known GenesZNF215
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027024
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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