A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433445



Internal ID21395447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43014341..43015171hg38UCSC Ensembl
chr22:43410347..43411177hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38831
hg19831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751507
SamplesNB11
Known GenesPACSIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433445
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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