A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881146



Internal ID22656120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50695239..50701544hg38UCSC Ensembl
chr22:51133667..51139972hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg386306
hg196306
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1414n209
Supporting Variantsnssv17484324
Samples
Known GenesSHANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881146
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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