A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011240



Internal ID18753774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12587682..12770129hg38UCSC Ensembl
Innerchr3:12629181..12811628hg19UCSC Ensembl
Innerchr3:12604181..12786628hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38182448
hg19182448
hg18182448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4686n100
Supporting Variantsnssv3591970
Samples
Known GenesRAF1, TMEM40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011240
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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