A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871023



Internal ID22645961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50664089..50666137hg38UCSC Ensembl
chr22:51102517..51104565hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg382049
hg192049
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871023
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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