A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612259



Internal ID21560564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187778496..187778496hg38UCSC Ensembl
chr3:187496284..187496284hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128948
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612259
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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