A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697416



Internal ID15105280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90097850..90099748hg38UCSC Ensembl
Innerchr9:90098748..90098850hg38UCSC Ensembl
Outerchr9:90096850..90100748hg38UCSC Ensembl
chr9:92860132..92862030hg19UCSC Ensembl
Innerchr9:92861030..92861132hg19UCSC Ensembl
Outerchr9:92859132..92863030hg19UCSC Ensembl
chr9:91899952..91901850hg18UCSC Ensembl
Innerchr9:91900952..91900850hg18UCSC Ensembl
Outerchr9:91898952..91902850hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3380801
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697416
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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