A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550163



Internal ID16337572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20548066..20573498hg38UCSC Ensembl
Innerchr10:20836995..20862427hg19UCSC Ensembl
Innerchr10:20877001..20902433hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3825433
hg1925433
hg1825433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv993n54
Supporting Variantsnssv1174155
SamplesHGDP01187
Known GenesMIR4675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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