A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669515



Internal ID21617820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20338388..20338388hg38UCSC Ensembl
chr22:20325911..20325911hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg383649
hg193649
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127104, nssv17133083
SamplesHG00732, NA12329
Known GenesLOC729444
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669515
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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