A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075272



Internal ID21414516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65364535..65371882hg38UCSC Ensembl
chr11:65132006..65139353hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387348
hg197348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591806
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075272
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer