A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677468



Internal ID15099010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89826799..89826812hg38UCSC Ensembl
Innerchr9:89826791..89826820hg38UCSC Ensembl
Outerchr9:89826778..89826833hg38UCSC Ensembl
chr9:92528246..92528259hg19UCSC Ensembl
Innerchr9:92528238..92528267hg19UCSC Ensembl
Outerchr9:92528225..92528280hg19UCSC Ensembl
chr9:91668066..91668079hg18UCSC Ensembl
Innerchr9:91668087..91668058hg18UCSC Ensembl
Outerchr9:91668045..91668100hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38239
hg19239
hg18239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3394550
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677468
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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