A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943287



Internal ID21363356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112331793..112331793hg38UCSC Ensembl
chr11:112202516..112202516hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192821
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943287
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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