A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857381



Internal ID22632316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45955086..45977900hg38UCSC Ensembl
chr10:51617936..51640757hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3822815
hg1922822
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464879
Samples
Known GenesTIMM23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857381
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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