A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550476



Internal ID16337885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38576045..38712472hg38UCSC Ensembl
Innerchr10:38869176..39005603hg19UCSC Ensembl
Innerchr10:38909182..39045609hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38136428
hg19136428
hg18136428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1053n54
Supporting Variantsnssv746947
Samples
Known GenesACTR3BP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550476
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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