A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607759



Internal ID21556064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186654334..186654334hg38UCSC Ensembl
chr3:186372123..186372123hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg386052
hg196052
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125057
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607759
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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