A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818232



Internal ID21263570
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 StatusM
Merged Variants
Supporting Variantsnssv13699089
Samples
Known GenesSNX30
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818232
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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