A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3365575



Internal ID15212552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64392514..64399812hg38UCSC Ensembl
Innerchr9:64393514..64398812hg38UCSC Ensembl
Outerchr9:64391514..64400812hg38UCSC Ensembl
chr9:69404932..69412230hg19UCSC Ensembl
Innerchr9:69405932..69411230hg19UCSC Ensembl
Outerchr9:69403932..69413230hg19UCSC Ensembl
chr9:68694752..68702050hg18UCSC Ensembl
Innerchr9:68695752..68701050hg18UCSC Ensembl
Outerchr9:68693752..68703050hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387299
hg197299
hg187299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697208
SamplesNA12878
Known GenesANKRD20A4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3365575
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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