A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789993



Internal ID21235331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33880255..33880255hg38UCSC Ensembl
chr11:33901801..33901801hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677635
Samples
Known GenesLMO2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789993
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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