A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863604



Internal ID22638539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133385575..133389949hg38UCSC Ensembl
chr10:135199079..135203453hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg384375
hg194375
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455624
Samples
Known GenesPAOX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863604
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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