A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7735839



Internal ID13385328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121464738..121465449hg38UCSC Ensembl
Outerchr9:121464538..121465649hg38UCSC Ensembl
Innerchr9:124227016..124227727hg19UCSC Ensembl
Outerchr9:124226816..124227927hg19UCSC Ensembl
Innerchr9:123266837..123267548hg18UCSC Ensembl
Outerchr9:123266637..123267748hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381112
hg191112
hg181112
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302935
Supporting Variants
SamplesNA12144
Known GenesGGTA1P
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7735839
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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