A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2914901



Internal ID10587881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15002143..15030143hg38UCSC Ensembl
Innerchr16:15096000..15124000hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3828001
hg1928001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7184468
SamplesHuRef
Known GenesPDXDC1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2914901
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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