A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931639



Internal ID21351708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119253539..119253539hg38UCSC Ensembl
chr11:119124249..119124249hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193152
SamplesHG002
Known GenesCBL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931639
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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