A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745731



Internal ID21389406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17876235..17878234hg38UCSC Ensembl
chr22:18359001..18361000hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433404
Supporting Variants
SamplesNB09
Known GenesMICAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745731
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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