A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv853119



Internal ID15800389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22379935..22438562hg38UCSC Ensembl
Innerchr16:22391256..22449883hg19UCSC Ensembl
Innerchr16:22298757..22357384hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3858628
hg1958628
hg1858628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571645
Supporting Variants
Samples
Known GenesRRN3P3, SMG1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv853119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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