A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036735



Internal ID18779266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133429369..133560087hg38UCSC Ensembl
Innerchr10:135242873..135373591hg19UCSC Ensembl
Innerchr10:135092863..135223581hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38130719
hg19130719
hg18130719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1001n100
Supporting Variantsnssv3706281, nssv3706285, nssv3520051, nssv3706287, nssv3511426, nssv3521468, nssv3507615, nssv3516810, nssv3706288, nssv3519459, nssv3504368, nssv3507028, nssv3706283, nssv3706280, nssv3514824, nssv3508426, nssv3518610, nssv3706290, nssv3706286, nssv3517226, nssv3516304, nssv3706282, nssv3706289, nssv3513162, nssv3706284
Samples
Known GenesCYP2E1, SCART1, SYCE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036735
Frequency
Sample Size29084
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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