A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017474



Internal ID18760008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3019068..3247215hg38UCSC Ensembl
Innerchr9:3019068..3247215hg19UCSC Ensembl
Innerchr9:3009068..3237215hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38228148
hg19228148
hg18228148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692367
Samples
Known GenesRFX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017474
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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