A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv177e180



Internal ID18981868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:147314354..147315434hg38UCSC Ensembl
chr7:147011446..147012526hg19UCSC Ensembl
chr7:146642379..146643459hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381081
hg191081
hg181081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv1005642, esv1001897
SamplesHuRef
Known GenesCNTNAP2, MIR548I4
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv177e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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