A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852266



Internal ID15799536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3656184..3668443hg38UCSC Ensembl
Innerchr16:3706185..3718444hg19UCSC Ensembl
Innerchr16:3646186..3658445hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812260
hg1912260
hg1812260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571258
Supporting Variants
Samples
Known GenesDNASE1, TRAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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