A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572688



Internal ID16360097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55808492..55811439hg38UCSC Ensembl
Innerchr16:55842404..55845351hg19UCSC Ensembl
Innerchr16:54399905..54402852hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg382948
hg192948
hg182948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv857719, nssv857718
Samples
Known GenesCES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572688
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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