A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951342



Internal ID22726707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17852304..17852370hg38UCSC Ensembl
chr22:18335070..18335136hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402693
Samples
Known GenesMICAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951342
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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