A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550407



Internal ID15991130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35631696..35641947hg38UCSC Ensembl
Innerchr10:35920624..35930875hg19UCSC Ensembl
Innerchr10:35960630..35970881hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3810252
hg1910252
hg1810252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1035n54
Supporting Variantsnssv746841
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550407
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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