A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711333



Internal ID21233094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42347250..42347250hg38UCSC Ensembl
chr8:42204768..42204768hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818529
Supporting Variants
Samples
Known GenesPOLB
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711333
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.887097


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