A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471289



Internal ID21128842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102444551..102445017hg38UCSC Ensembl
chr11:102315282..102315748hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985477
Samples
Known GenesTMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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