A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296318



Internal ID20505536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24812021..24812021hg38UCSC Ensembl
chr22:25207988..25207988hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761173
Supporting Variants
Samples
Known GenesSGSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296318
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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