A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853502



Internal ID22628437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98391063..98397052hg38UCSC Ensembl
chr13:99043317..99049306hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg385990
hg195990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453756
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853502
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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