A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039326



Internal ID18781857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90836574..90923447hg38UCSC Ensembl
Innerchr9:93598856..93685729hg19UCSC Ensembl
Innerchr9:92638677..92725550hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3886874
hg1986874
hg1886874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7687n100
Supporting Variantsnssv3759784
Samples
Known GenesSYK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039326
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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