A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851857



Internal ID15799127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:790597..847566hg38UCSC Ensembl
Innerchr16:840597..897566hg19UCSC Ensembl
Innerchr16:780598..837567hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3856970
hg1956970
hg1856970
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571045
Supporting Variants
Samples
Known GenesCHTF18, GNG13, PRR25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851857
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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