A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3407895



Internal ID14908171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132376744..132378842hg38UCSC Ensembl
Innerchr9:132377744..132377842hg38UCSC Ensembl
Outerchr9:132375744..132379842hg38UCSC Ensembl
chr9:135252131..135254229hg19UCSC Ensembl
Innerchr9:135253131..135253229hg19UCSC Ensembl
Outerchr9:135251131..135255229hg19UCSC Ensembl
chr9:134241952..134244050hg18UCSC Ensembl
Innerchr9:134242952..134243050hg18UCSC Ensembl
Outerchr9:134240952..134245050hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4531e59
Supporting Variantsessv8696537
SamplesNA19240
Known GenesTTF1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3407895
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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