A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565817



Internal ID21514133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65884745..65884794hg38UCSC Ensembl
chr5:65180573..65180622hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152203
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565817
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