A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3450767



Internal ID15297715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64462457..64465956hg38UCSC Ensembl
Innerchr9:64463457..64464955hg38UCSC Ensembl
Outerchr9:64461457..64466956hg38UCSC Ensembl
chr9:43030956..43034454hg19UCSC Ensembl
Innerchr9:43031956..43033454hg19UCSC Ensembl
Outerchr9:43029956..43035454hg19UCSC Ensembl
chr9:43020952..43024450hg18UCSC Ensembl
Innerchr9:43021952..43023450hg18UCSC Ensembl
Outerchr9:43019952..43025450hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383500
hg193499
hg183499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696814
SamplesNA19240
Known GenesFAM95B1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3450767
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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