A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879137



Internal ID22654105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78427900..78435048hg38UCSC Ensembl
chr16:78461797..78468945hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg387149
hg197149
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479679
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879137
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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