A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868563



Internal ID22643499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31441887..31447386hg38UCSC Ensembl
chr22:31837873..31843372hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482858
Samples
Known GenesEIF4ENIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868563
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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