A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052033



Internal ID19141252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133403671..133456451hg38UCSC Ensembl
Innerchr10:135217175..135269955hg19UCSC Ensembl
Innerchr10:135067165..135119945hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3852781
hg1952781
hg1852781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521981
Samples
Known GenesMTG1, SCART1, SPRN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052033
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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