A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648213



Internal ID21596518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12262175..12262175hg38UCSC Ensembl
chr18:12262174..12262174hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100152
SamplesHG03486
Known GenesCIDEA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648213
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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