A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649986



Internal ID21598291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101737016..101737016hg38UCSC Ensembl
chr13:102389366..102389366hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089064
SamplesHG00731
Known GenesFGF14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649986
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer