A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869152



Internal ID22644087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50126559..50155544hg38UCSC Ensembl
chr22:50564988..50593973hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3828986
hg1928986
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484283
Samples
Known GenesMOV10L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869152
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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