A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567733



Internal ID21516072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109341560..109341784hg38UCSC Ensembl
chr5:108677261..108677485hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126323
SamplesHG03486
Known GenesPJA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567733
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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