A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885857



Internal ID22660843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36987105..37007601hg38UCSC Ensembl
chr22:37383146..37403642hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3820497
hg1920497
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482928
Samples
Known GenesTEX33
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885857
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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