A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028160



Internal ID21937503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45753584..45774973hg38UCSC Ensembl
chr11:45775135..45796524hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3821390
hg1921390
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589050
Samples
Known GenesDKFZp779M0652
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028160
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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