A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572651



Internal ID16360060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55762760..55788619hg38UCSC Ensembl
Innerchr16:55796672..55822531hg19UCSC Ensembl
Innerchr16:54354173..54380032hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3825860
hg1925860
hg1825860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5126n54
Supporting Variantsnssv857551, nssv857552
Samples
Known GenesCES1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572651
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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