A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3411011



Internal ID15257971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89826787..89826806hg38UCSC Ensembl
Innerchr9:89826783..89826810hg38UCSC Ensembl
Outerchr9:89826764..89826829hg38UCSC Ensembl
chr9:92528234..92528253hg19UCSC Ensembl
Innerchr9:92528230..92528257hg19UCSC Ensembl
Outerchr9:92528211..92528276hg19UCSC Ensembl
chr9:91668054..91668073hg18UCSC Ensembl
Innerchr9:91668077..91668050hg18UCSC Ensembl
Outerchr9:91668031..91668096hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8679454
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3411011
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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