A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849924



Internal ID22624859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102038657..102040744hg38UCSC Ensembl
chr13:102691007..102693094hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463390
Samples
Known GenesFGF14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849924
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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