A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621281



Internal ID21569586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:226048..226048hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38709
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166665
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621281
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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