A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041989



Internal ID19131208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130589752..130618610hg38UCSC Ensembl
Innerchr9:133465139..133493997hg19UCSC Ensembl
Innerchr9:132454960..132483818hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3828859
hg1928859
hg1828859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695281
Samples
Known GenesFUBP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041989
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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