A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755026



Internal ID20530886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26661895..26661895hg38UCSC Ensembl
chr22:27057859..27057859hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279726
Samples
Known GenesMIAT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755026
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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