A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760760



Internal ID20536620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17754012..17754012hg38UCSC Ensembl
chr22:18236778..18236778hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276653
Samples
Known GenesBID
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760760
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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