A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943866



Internal ID21363935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131519274..131519274hg38UCSC Ensembl
chr11:131389168..131389168hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193161
SamplesHG002
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943866
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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