A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581498



Internal ID21529997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176326341..176326464hg38UCSC Ensembl
chr3:176044129..176044252hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126839
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581498
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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