A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851805



Internal ID22626740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92493424..92494623hg38UCSC Ensembl
chr14:92959768..92960967hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470353
Samples
Known GenesSLC24A4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851805
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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