A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579877



Internal ID21528361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122477998..122478557hg38UCSC Ensembl
chr3:122196845..122197404hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124402
SamplesNA20847
Known GenesKPNA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579877
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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