A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031459



Internal ID18773993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6216913..6657192hg38UCSC Ensembl
Innerchr9:6216913..6657192hg19UCSC Ensembl
Innerchr9:6206913..6647192hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38440280
hg19440280
hg18440280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7386n100
Supporting Variantsnssv3758101
Samples
Known GenesGLDC, IL33, TPD52L3, UHRF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031459
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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