A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585812



Internal ID21534360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46014684..46015030hg38UCSC Ensembl
chr11:46036235..46036581hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074726
SamplesHG00732
Known GenesPHF21A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585812
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