A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573354



Internal ID21521757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40712255..40712936hg38UCSC Ensembl
chr3:40753746..40754427hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130512
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573354
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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