A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660711



Internal ID21609016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26856630..26856630hg38UCSC Ensembl
chr18:24436594..24436594hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100827
SamplesHG02587
Known GenesAQP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660711
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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