A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818791



Internal ID21264129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3504672..3504672hg38UCSC Ensembl
chr9:3504672..3504672hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707205, nssv13710297
Samples
Known GenesRFX3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818791
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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