A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680778



Internal ID21202637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108689609..108689609hg38UCSC Ensembl
chr1:109232231..109232231hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680778
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.96875


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