A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645134



Internal ID21593439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131865893..131865893hg38UCSC Ensembl
chr11:131735787..131735787hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073272
SamplesHG00731
Known GenesNTM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645134
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