A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863123



Internal ID22638058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22372432..22377087hg38UCSC Ensembl
chr10:22661361..22666016hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384656
hg194656
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460005
Samples
Known GenesSPAG6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863123
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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