A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699089



Internal ID21220939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112866854..112866854hg38UCSC Ensembl
chr9:115629134..115629134hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818232
Supporting Variants
Samples
Known GenesSNX30
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699089
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.909091


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