A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039781



Internal ID21949124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117310194..117312214hg38UCSC Ensembl
chr11:117180910..117182930hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382021
hg192021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605650
Samples
Known GenesBACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039781
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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