A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040509



Internal ID18783040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43066585..43095201hg38UCSC Ensembl
Innerchr10:43562033..43590649hg19UCSC Ensembl
Innerchr10:42882039..42910655hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3828617
hg1928617
hg1828617
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv724n100
Supporting Variantsnssv3507720
Samples
Known GenesRET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040509
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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