A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931391



Internal ID21351460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121114637..121114637hg38UCSC Ensembl
chr11:120985346..120985346hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192348
SamplesHG002
Known GenesTECTA
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931391
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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