A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863386



Internal ID22638321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97703577..97707369hg38UCSC Ensembl
chr14:98169914..98173706hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383793
hg193793
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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