A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571041



Internal ID16011764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:774098..828324hg38UCSC Ensembl
Innerchr16:824098..878324hg19UCSC Ensembl
Innerchr16:764099..818325hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3854227
hg1954227
hg1854227
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4828n54
Supporting Variantsnssv851853
Samples
Known GenesCHTF18, GNG13, PRR25, RPUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571041
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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