A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668327



Internal ID21616632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29907437..29907437hg38UCSC Ensembl
chr22:30303426..30303426hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135211
SamplesNA19238
Known GenesMTMR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668327
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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