A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652084



Internal ID21600389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62046486..62046486hg38UCSC Ensembl
chr18:59713719..59713719hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101750
SamplesHG00732
Known GenesPIGN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652084
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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