A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853695



Internal ID22628630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98296509..98311127hg38UCSC Ensembl
chr13:98948763..98963381hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3814619
hg1914619
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459656
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853695
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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