A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4014e59



Internal ID22765234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157562998..157563996hg38UCSC Ensembl
chr7:157355691..157356689hg19UCSC Ensembl
chr7:157048452..157049450hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3432861, esv3369863
SamplesNA19239, NA19240
Known GenesPTPRN2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4014e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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