A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066077



Internal ID18808608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88916836..89035141hg38UCSC Ensembl
Innerchr16:88983244..89101549hg19UCSC Ensembl
Innerchr16:87510745..87629050hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38118306
hg19118306
hg18118306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719125
Samples
Known GenesCBFA2T3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066077
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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