A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873750



Internal ID22648698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21850800..21855862hg38UCSC Ensembl
chr22:22205089..22210151hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg385063
hg195063
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489496
Samples
Known GenesMAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873750
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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