A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875554



Internal ID22650512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31525889..31527563hg38UCSC Ensembl
chr22:31921875..31923549hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381675
hg191675
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482862, nssv17482861
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875554
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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