A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3446655



Internal ID15293605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64411056..64421045hg38UCSC Ensembl
Innerchr9:64412062..64420046hg38UCSC Ensembl
Outerchr9:64410058..64422044hg38UCSC Ensembl
chr9:43082056..43092054hg19UCSC Ensembl
Innerchr9:43083056..43091054hg19UCSC Ensembl
Outerchr9:43081056..43093054hg19UCSC Ensembl
chr9:43072052..43082050hg18UCSC Ensembl
Innerchr9:43073052..43081050hg18UCSC Ensembl
Outerchr9:43071052..43083050hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg389990
hg199999
hg189999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696825
SamplesNA12892
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3446655
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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