A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053793



Internal ID19143012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..108612hg38UCSC Ensembl
Innerchr10:72797..154552hg19UCSC Ensembl
Innerchr10:62797..144552hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3881752
hg1981756
hg1881756
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n100
Supporting Variantsnssv3483807, nssv3492826, nssv3493709
Samples
Known GenesTUBB8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053793
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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