A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645453



Internal ID21593758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54817..54817hg38UCSC Ensembl
chr18:54817..54817hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101824
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645453
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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