A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044985



Internal ID18787516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133444034..133551831hg38UCSC Ensembl
Innerchr10:135257538..135365335hg19UCSC Ensembl
Innerchr10:135107528..135215325hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38107798
hg19107798
hg18107798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1001n100
Supporting Variantsnssv3511498
Samples
Known GenesCYP2E1, SCART1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044985
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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