A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569803



Internal ID21518165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108468739..108476017hg38UCSC Ensembl
chr5:107804440..107811718hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg387279
hg197279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119643
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569803
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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