A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665766



Internal ID21614072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31495982..31495982hg38UCSC Ensembl
chr22:31891968..31891968hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38764
hg19764
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138174
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665766
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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