A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581899



Internal ID21530404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67782189..67782518hg38UCSC Ensembl
chr3:67832613..67832942hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121371
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581899
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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