A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572750



Internal ID21521143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135827660..135827790hg38UCSC Ensembl
chr5:135163349..135163479hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126759
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572750
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