A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653688



Internal ID21601993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:131100..131100hg38UCSC Ensembl
chr11:186341..186341hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086453
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653688
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