A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789871



Internal ID21235209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119253540..119253540hg38UCSC Ensembl
chr11:119124250..119124250hg19UCSC 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 Variantsnssv13702125
Samples
Known GenesCBL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789871
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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