A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602678



Internal ID21551337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120129631..120131722hg38UCSC Ensembl
chr11:120000339..120002430hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382092
hg192092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072891
SamplesHG03732
Known GenesTRIM29
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602678
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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