A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860519



Internal ID22635454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102384799..102387123hg38UCSC Ensembl
chr14:102851136..102853460hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382325
hg192325
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459973
Samples
Known GenesTECPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860519
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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