A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572664



Internal ID16360073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55768226..55793775hg38UCSC Ensembl
Innerchr16:55802138..55827687hg19UCSC Ensembl
Innerchr16:54359639..54385188hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3825550
hg1925550
hg1825550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5129n54
Supporting Variantsnssv857595, nssv857594
Samples
Known GenesCES1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572664
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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