A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572928



Internal ID16013651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70154371..70173267hg38UCSC Ensembl
Innerchr16:70188274..70207170hg19UCSC Ensembl
Innerchr16:68745775..68764671hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3818897
hg1918897
hg1818897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859096
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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