A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515826



Internal ID15442883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11650504..11653506hg38UCSC Ensembl
Innerchr1:11710561..11713563hg19UCSC Ensembl
Innerchr1:11633148..11636150hg18UCSC Ensembl
Innerchr1:11644827..11647829hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383003
hg193003
hg183003
hg173003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664907, nssv681520, nssv683681, nssv693798, nssv655395, nssv660113, nssv682473, nssv682277, nssv666865, nssv679392, nssv685412, nssv674188, nssv673329
Samples
Known GenesFBXO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515826
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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