A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059098



Internal ID18801629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56733938..57028336hg38UCSC Ensembl
Innerchr16:56767850..57062248hg19UCSC Ensembl
Innerchr16:55325351..55619749hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38294399
hg19294399
hg18294399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559351
Samples
Known GenesCETP, HERPUD1, MIR138-2, MIR6863, NLRC5, NUP93, SLC12A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059098
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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