A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574203



Internal ID21522615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49186563..49196829hg38UCSC Ensembl
chr3:49223996..49234262hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3810267
hg1910267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132895
SamplesHG03065
Known GenesC3orf84
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574203
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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