A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886933



Internal ID22661922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17505671..17506670hg38UCSC Ensembl
chr22:17984703..17985702hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481456
Samples
Known GenesCECR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886933
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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