A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3427865



Internal ID15274821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89058017..89061415hg38UCSC Ensembl
Innerchr9:89059017..89060415hg38UCSC Ensembl
Outerchr9:89057017..89062415hg38UCSC Ensembl
chr9:91672932..91676330hg19UCSC Ensembl
Innerchr9:91673932..91675330hg19UCSC Ensembl
Outerchr9:91671932..91677330hg19UCSC Ensembl
chr9:90862752..90866150hg18UCSC Ensembl
Innerchr9:90863752..90865150hg18UCSC Ensembl
Outerchr9:90861752..90867150hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383399
hg193399
hg183399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4473e59
Supporting Variantsessv8697412
SamplesNA19240
Known GenesSHC3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3427865
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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