A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3386776



Internal ID15233745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88625325..88627080hg38UCSC Ensembl
Innerchr9:88625325..88627080hg38UCSC Ensembl
Outerchr9:88625323..88627103hg38UCSC Ensembl
chr9:91240240..91241995hg19UCSC Ensembl
Innerchr9:91240240..91241995hg19UCSC Ensembl
Outerchr9:91240238..91242018hg19UCSC Ensembl
chr9:90430060..90431815hg18UCSC Ensembl
Innerchr9:90430060..90431815hg18UCSC Ensembl
Outerchr9:90430058..90431838hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381756
hg191756
hg181756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652446
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3386776
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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