A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3394550



Internal ID15241515
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 StatusM
Merged Variants
Supporting Variantsessv8677469, essv8677468
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3394550
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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