A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662522



Internal ID21610827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62278583..62278583hg38UCSC Ensembl
chr18:59945816..59945816hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381865
hg191865
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101557
SamplesHG03732
Known GenesKIAA1468
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662522
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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