A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645926



Internal ID21594231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48860469..48860469hg38UCSC Ensembl
chr18:46386840..46386840hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101164
SamplesHG03009
Known GenesCTIF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645926
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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