A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7838587



Internal ID15007176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91510807..91510808hg38UCSC Ensembl
Innerchr9:91510777..91510838hg38UCSC Ensembl
Outerchr9:91510776..91510839hg38UCSC Ensembl
chr9:94273089..94273090hg19UCSC Ensembl
Innerchr9:94273059..94273120hg19UCSC Ensembl
Outerchr9:94273058..94273121hg19UCSC Ensembl
chr9:93312910..93312911hg18UCSC Ensembl
Innerchr9:93312941..93312880hg18UCSC Ensembl
Outerchr9:93312879..93312942hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38272
hg19272
hg18272
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308576
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7838587
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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