A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7749257



Internal ID14009826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17274291..17274292hg38UCSC Ensembl
Innerchr9:17274234..17274349hg38UCSC Ensembl
Outerchr9:17274233..17274350hg38UCSC Ensembl
chr9:17274289..17274290hg19UCSC Ensembl
Innerchr9:17274232..17274347hg19UCSC Ensembl
Outerchr9:17274231..17274348hg19UCSC Ensembl
chr9:17264289..17264290hg18UCSC Ensembl
Innerchr9:17264347..17264232hg18UCSC Ensembl
Outerchr9:17264231..17264348hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38179
hg19179
hg18179
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3304113
Supporting Variants
SamplesNA18856
Known GenesCNTLN
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7749257
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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