A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667176



Internal ID9933281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109356665..109361756hg38UCSC Ensembl
Outerchr9:109356508..109361909hg38UCSC Ensembl
Innerchr9:112118945..112124036hg19UCSC Ensembl
Outerchr9:112118788..112124189hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385402
hg195402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6040367, essv5528178
SamplesNA18574, HG00513
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667176
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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