A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652460



Internal ID21600765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125139098..125139098hg38UCSC Ensembl
chr11:125008994..125008994hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072939
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652460
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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