A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101306



Internal ID22010539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17147358..17147358hg38UCSC Ensembl
chr22:17628248..17628248hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643291
Samples
Known GenesCECR5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101306
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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