A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659200



Internal ID21607505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:43793880..43793880hg38UCSC Ensembl
chr18:41373845..41373845hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101614
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659200
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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