A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859110



Internal ID22634045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:118637368..118638593hg38UCSC Ensembl
chr8:119649607..119650832hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505664, nssv17505665
Samples
Known GenesSAMD12-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859110
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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