A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550164



Internal ID16337573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20548066..20576228hg38UCSC Ensembl
Innerchr10:20836995..20865157hg19UCSC Ensembl
Innerchr10:20877001..20905163hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3828163
hg1928163
hg1828163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv993n54
Supporting Variantsnssv1174156
SamplesHGDP01103
Known GenesMIR4675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550164
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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