A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645349



Internal ID21593654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121114637..121114637hg38UCSC Ensembl
chr11:120985346..120985346hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073037
SamplesHG00731
Known GenesTECTA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645349
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