A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv14e196



Internal ID20123213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6710054..6986820hg38UCSC Ensembl
chr19:6710065..6986831hg19UCSC Ensembl
chr19:6661065..6937831hg18UCSC Ensembl
chr19:6661065..6937831hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38276767
hg19276767
hg18276767
hg17276767
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2422461, esv2422507, esv2422286
SamplesND01570, ND03660, ND01205
Known GenesC3, EMR1, EMR4P, GPR108, MIR6791, SH2D3A, TRIP10, VAV1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)dgv14e196
Frequency
Sample Size181
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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