A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646902



Internal ID21838949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20877189..20877189hg38UCSC Ensembl
chr22:21231477..21231477hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110473
Supporting Variants
Samples
Known GenesSNAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646902
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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