A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943759



Internal ID21363828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13016508..13016508hg38UCSC Ensembl
chr11:13038055..13038055hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190799
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943759
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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