A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3757e59



Internal ID22764977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26212207..26213405hg38UCSC Ensembl
chr7:26251827..26253025hg19UCSC Ensembl
chr7:26218352..26219550hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3387859, esv3383527
SamplesNA12891, NA12878
Known GenesCBX3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3757e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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