A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704964



Internal ID21226777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93818393..93818393hg38UCSC Ensembl
chr9:96580675..96580675hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704964
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.129032


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