A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688653



Internal ID21210508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11112830..11112830hg38UCSC Ensembl
chr2:11252956..11252956hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2805117
Supporting Variants
Samples
Known GenesFLJ33534
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688653
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.806452


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