A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853665



Internal ID22628600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93136977..93138576hg38UCSC Ensembl
chr14:93603322..93604921hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853665
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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