A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578622



Internal ID21527093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101802363..101802921hg38UCSC Ensembl
chr3:101521207..101521765hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130537
SamplesHG03486
Known GenesNXPE3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578622
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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