A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665286



Internal ID21613591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31982579..31982579hg38UCSC Ensembl
chr22:32378566..32378566hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127742
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665286
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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