A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573367



Internal ID21521771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139363182..139363643hg38UCSC Ensembl
chr5:138698871..138699332hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139567
SamplesHG03486
Known GenesPAIP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573367
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