A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661915



Internal ID21610220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127033277..127033277hg38UCSC Ensembl
chr11:126903172..126903172hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073093
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661915
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