A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4522e59



Internal ID22765742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121464623..121465549hg38UCSC Ensembl
chr9:124226901..124227827hg19UCSC Ensembl
chr9:123266722..123267648hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38927
hg19927
hg18927
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302935, esv3302557
SamplesNA10851, NA12751, NA18504, NA18870, NA07346, NA12891, NA11992, NA12761, NA12044, NA12003, NA12878, NA18516, NA19114, NA11919, NA12249, NA12144, NA12716, NA07051, NA06986, NA12749, NA12006, NA07000
Known GenesGGTA1P
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4522e59
Frequency
Sample Size185
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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