A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572919



Internal ID16013642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70141045..70159293hg38UCSC Ensembl
Innerchr16:70174948..70193196hg19UCSC Ensembl
Innerchr16:68732449..68750697hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3818249
hg1918249
hg1818249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5179n54
Supporting Variantsnssv859086
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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