A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571760



Internal ID21520142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197785471..197785577hg38UCSC Ensembl
chr3:197512342..197512448hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137596
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571760
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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