A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572925



Internal ID16013648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70151833..70162281hg38UCSC Ensembl
Innerchr16:70185736..70196184hg19UCSC Ensembl
Innerchr16:68743237..68753685hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3810449
hg1910449
hg1810449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5180n54
Supporting Variantsnssv859093
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572925
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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