A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943025



Internal ID21363095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116812456..116812456hg38UCSC Ensembl
chr11:116683172..116683172hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193135
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943025
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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