A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658993



Internal ID21607298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44663739..44663739hg38UCSC Ensembl
chr11:44685289..44685289hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074694
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658993
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