A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875316



Internal ID22650273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88137378..88140970hg38UCSC Ensembl
chr16:88170984..88174576hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383593
hg193593
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474166, nssv17474167, nssv17479750, nssv17474165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875316
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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