A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552732



Internal ID16340141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133560415..133566430hg38UCSC Ensembl
Innerchr10:135373919..135379934hg19UCSC Ensembl
Innerchr10:135223909..135229924hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386016
hg196016
hg186016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763006
Samples
Known GenesSYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552732
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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