A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870778



Internal ID22645714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50623466..50626842hg38UCSC Ensembl
chr22:51061894..51065270hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg383377
hg193377
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484296
Samples
Known GenesARSA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870778
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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