A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935828



Internal ID21355897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50316936..50316936hg38UCSC Ensembl
chr22:50755365..50755365hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188813
SamplesHG002
Known GenesDENND6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935828
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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