A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659870



Internal ID21608175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25537316..25537316hg38UCSC Ensembl
chr11:25558862..25558862hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073891
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659870
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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