A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657264



Internal ID21605569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27239383..27239383hg38UCSC Ensembl
chr17:25566409..25566409hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085876
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657264
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