A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696971



Internal ID13732289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62407855..62417153hg38UCSC Ensembl
Innerchr9:62408855..62416153hg38UCSC Ensembl
Outerchr9:62406855..62418153hg38UCSC Ensembl
chr9:46719156..46728454hg19UCSC Ensembl
Innerchr9:46720156..46727454hg19UCSC Ensembl
Outerchr9:46718156..46729454hg19UCSC Ensembl
chr9:46559152..46568450hg18UCSC Ensembl
Innerchr9:46560152..46567450hg18UCSC Ensembl
Outerchr9:46558152..46569450hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg389299
hg199299
hg189299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3423185
Supporting Variants
SamplesNA12892
Known GenesKGFLP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696971
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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