A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667290



Internal ID21615597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27051912..27051912hg38UCSC Ensembl
chr22:27447874..27447874hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122601
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667290
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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