A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051646



Internal ID18794177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43074511..43095726hg38UCSC Ensembl
Innerchr10:43569959..43591174hg19UCSC Ensembl
Innerchr10:42889965..42911180hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3821216
hg1921216
hg1821216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv725n100
Supporting Variantsnssv3520573
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)nsv1051646
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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