A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047838



Internal ID19137057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42739142..42883771hg38UCSC Ensembl
Innerchr10:43234590..43379219hg19UCSC Ensembl
Innerchr10:42554596..42699225hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38144630
hg19144630
hg18144630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514347
Samples
Known GenesBMS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047838
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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