A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050563



Internal ID18793094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43079488..43095609hg38UCSC Ensembl
Innerchr10:43574936..43591057hg19UCSC Ensembl
Innerchr10:42894942..42911063hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3816122
hg1916122
hg1816122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv726n100
Supporting Variantsnssv3504415, nssv3502835, nssv3509363, nssv3521993, nssv3516595
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)nsv1050563
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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