A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863573



Internal ID22638508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64421331..64423861hg38UCSC Ensembl
chr14:64888049..64890579hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg382531
hg192531
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450215
Samples
Known GenesMIR548AZ, MTHFD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863573
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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