A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848540



Internal ID22623475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102066308..102072431hg38UCSC Ensembl
chr13:102718658..102724781hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg386124
hg196124
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449957
Samples
Known GenesFGF14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848540
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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