A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859097



Internal ID15806367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70156498..70162547hg38UCSC Ensembl
Innerchr16:70190401..70196450hg19UCSC Ensembl
Innerchr16:68747902..68753951hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386050
hg196050
hg186050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572929
Supporting Variants
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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