A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566563



Internal ID21514891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43088616..43088668hg38UCSC Ensembl
chr5:43088718..43088770hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130007
SamplesNA19238
Known GenesLOC100506639
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566563
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