A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811100



Internal ID21256438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1273317..1273317hg38UCSC Ensembl
chr5:1273432..1273432hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704250
Samples
Known GenesTERT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811100
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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