A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871541



Internal ID22646479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31537944..31541650hg38UCSC Ensembl
chr22:31933930..31937636hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg383707
hg193707
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482864
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871541
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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