A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667041



Internal ID21615348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20338539..20338539hg38UCSC Ensembl
chr22:20326062..20326062hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381311
hg191311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133284
SamplesHG03486
Known GenesLOC729444
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667041
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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