A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655810



Internal ID21604115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49799390..49799390hg38UCSC Ensembl
chr13:50373526..50373526hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095660, nssv17081541, nssv17086243
SamplesHG00731, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655810
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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