A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855887



Internal ID22630822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42783508..42814782hg38UCSC Ensembl
chr13:43357644..43388918hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3831275
hg1931275
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453103
Samples
Known GenesFAM216B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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