A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892797



Internal ID18836931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15031584..15104346hg38UCSC Ensembl
Outerchr16:15031584..15104346hg38UCSC Ensembl
Innerchr16:15125441..15198203hg19UCSC Ensembl
Outerchr16:15125441..15198203hg19UCSC Ensembl
Innerchr16:15032942..15105704hg18UCSC Ensembl
Outerchr16:15032942..15105704hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3872763
hg1972763
hg1872763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789311
Samples
Known GenesNTAN1, PDXDC1, RRN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892797
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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