A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687318



Internal ID21209173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1934280..1934280hg38UCSC Ensembl
chr1:1865719..1865719hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801113
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687318
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.703125


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