A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851855



Internal ID15799125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:787857..798755hg38UCSC Ensembl
Innerchr16:837857..848755hg19UCSC Ensembl
Innerchr16:777858..788756hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810899
hg1910899
hg1810899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571043
Supporting Variants
Samples
Known GenesCHTF18, GNG13, RPUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851855
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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