A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3731e59



Internal ID22764951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:653289..655287hg38UCSC Ensembl
chr7:692926..694924hg19UCSC Ensembl
chr7:659452..661450hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3409643, esv3357138
SamplesNA19239, NA19240
Known GenesPRKAR1B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3731e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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