A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954859



Internal ID21374928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134055477..134055477hg38UCSC Ensembl
chr11:133925372..133925372hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193184
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954859
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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