A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610226



Internal ID21558531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160312973..160312973hg38UCSC Ensembl
chr3:160030761..160030761hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124394
SamplesHG03065
Known GenesIFT80
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610226
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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