A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618079



Internal ID21566384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111573692..111573692hg38UCSC Ensembl
chr3:111292539..111292539hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130291
SamplesHG00096
Known GenesCD96
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618079
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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