A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032573



Internal ID21941916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78877446..78880064hg38UCSC Ensembl
chr11:78588491..78591109hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382619
hg192619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583500
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032573
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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