A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858067



Internal ID22633002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49703470..49704669hg38UCSC Ensembl
chr12:50097253..50098452hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455824, nssv17463815
Samples
Known GenesFMNL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858067
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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