A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615518



Internal ID21563823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186401634..186401634hg38UCSC Ensembl
chr3:186119423..186119423hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130308
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615518
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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