A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv166e180



Internal ID22757576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31550773..31552390hg38UCSC Ensembl
chr7:31590387..31592004hg19UCSC Ensembl
chr7:31556912..31558529hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381618
hg191618
hg181618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv1005712, esv993805
SamplesHuRef
Known GenesCCDC129
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv166e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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