A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029822



Internal ID21939165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118679093..118690934hg38UCSC Ensembl
chr11:118549802..118561643hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3811842
hg1911842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603204
Samples
Known GenesTREH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029822
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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