A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8945257



Internal ID13886123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83070103..83070146hg38UCSC Ensembl
Innerchr9:83070121..83070128hg38UCSC Ensembl
Outerchr9:83070078..83070171hg38UCSC Ensembl
chr9:85685018..85685061hg19UCSC Ensembl
Innerchr9:85685036..85685043hg19UCSC Ensembl
Outerchr9:85684993..85685086hg19UCSC Ensembl
chr9:84874838..84874881hg18UCSC Ensembl
Innerchr9:84874863..84874856hg18UCSC Ensembl
Outerchr9:84874813..84874906hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38256
hg19256
hg18256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3439047
Supporting Variants
SamplesNA18519
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8945257
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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