A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860463



Internal ID22635398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98896857..98898881hg38UCSC Ensembl
chr14:99363194..99365218hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382025
hg192025
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470405, nssv17470236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860463
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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