A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040490



Internal ID19129709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19590532..19656610hg38UCSC Ensembl
Innerchr16:19601854..19667932hg19UCSC Ensembl
Innerchr16:19509355..19575433hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3866079
hg1966079
hg1866079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716935
Samples
Known GenesC16orf62
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040490
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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