A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039499



Internal ID21948842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13331501..13334149hg38UCSC Ensembl
chr11:13353048..13355696hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579701
Samples
Known GenesARNTL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039499
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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