A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279726



Internal ID20488944
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 StatusS
Merged Variantsnsv4755026
Supporting Variants
Samples
Known GenesMIAT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279726
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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