A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946786



Internal ID21366855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126276308..126276308hg38UCSC Ensembl
chr11:126146203..126146203hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192830
SamplesHG002
Known GenesFOXRED1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946786
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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