A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764035



Internal ID20539895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26601649..26601649hg38UCSC Ensembl
chr22:26997613..26997613hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268582
Samples
Known GenesCRYBB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764035
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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