A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638016



Internal ID6678114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14986410..15011256hg38UCSC Ensembl
chr16:15080267..15105113hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3824847
hg1924847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv481e214
Supporting Variantsessv15383456, essv15383463, essv15383450, essv15383462, essv15383457, essv15383464, essv15383465, essv15383466, essv15383454, essv15383467, essv15383459, essv15383461, essv15383453, essv15383451, essv15383452, essv15383458, essv15383460, essv15383455
SamplesNA21099, HG00766, HG02888, NA18944, HG01501, NA21098, HG02219, NA21142, HG01204, NA21143, NA21117, NA19256, HG01685, HG01375, NA20786, HG01468, HG03072, HG04161
Known GenesPDXDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638016
Frequency
Sample Size2504
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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