A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552665



Internal ID15993388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133429089..133567238hg38UCSC Ensembl
Innerchr10:135242593..135380742hg19UCSC Ensembl
Innerchr10:135092583..135230732hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38138150
hg19138150
hg18138150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1487n54
Supporting Variantsnssv762710
Samples
Known GenesCYP2E1, SCART1, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552665
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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