A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581995



Internal ID21530502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98406643..98412478hg38UCSC Ensembl
chr3:98125487..98131322hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg385836
hg195836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120742
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581995
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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