A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3451863



Internal ID14952122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86052717..86054115hg38UCSC Ensembl
Innerchr9:86053115..86053717hg38UCSC Ensembl
Outerchr9:86051717..86055115hg38UCSC Ensembl
chr9:88667632..88669030hg19UCSC Ensembl
Innerchr9:88668030..88668632hg19UCSC Ensembl
Outerchr9:88666632..88670030hg19UCSC Ensembl
chr9:87857452..87858850hg18UCSC Ensembl
Innerchr9:87858452..87857850hg18UCSC Ensembl
Outerchr9:87856452..87859850hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4465e59
Supporting Variantsessv8697395
SamplesNA19240
Known GenesGOLM1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3451863
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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