A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583434



Internal ID21531959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11108480..11108844hg38UCSC Ensembl
chr2:11248606..11248970hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17108035
SamplesHG00731
Known GenesFLJ33534
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583434
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