A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697428



Internal ID14758715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91904849..91905747hg38UCSC Ensembl
Innerchr9:91904848..91905748hg38UCSC Ensembl
Outerchr9:91903849..91906747hg38UCSC Ensembl
chr9:94667131..94668029hg19UCSC Ensembl
Innerchr9:94667130..94668030hg19UCSC Ensembl
Outerchr9:94666131..94669029hg19UCSC Ensembl
chr9:93706952..93707850hg18UCSC Ensembl
Innerchr9:93707851..93706951hg18UCSC Ensembl
Outerchr9:93705952..93708850hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3347273
Supporting Variants
SamplesNA19240
Known GenesROR2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697428
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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