A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866214



Internal ID22641149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98364475..98441693hg38UCSC Ensembl
chr13:99016729..99093947hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3877219
hg1977219
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454795
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866214
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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