A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660904



Internal ID21609209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75586036..75586036hg38UCSC Ensembl
chr11:75297081..75297081hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075892
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660904
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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