A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051312



Internal ID19140531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20177798..20261048hg38UCSC Ensembl
Innerchr16:20189120..20272370hg19UCSC Ensembl
Innerchr16:20096621..20179871hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3883251
hg1983251
hg1883251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3547110, nssv3547109
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051312
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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