A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667129



Internal ID21615436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38398927..38398927hg38UCSC Ensembl
chr22:38794932..38794932hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123516
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667129
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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