A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110608



Internal ID22019841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50319567..50319567hg38UCSC Ensembl
chr22:50757996..50757996hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645985
Samples
Known GenesDENND6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110608
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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