A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676899



Internal ID9596318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91298923..91302133hg38UCSC Ensembl
Outerchr9:91298886..91302183hg38UCSC Ensembl
Innerchr9:94061205..94064415hg19UCSC Ensembl
Outerchr9:94061168..94064465hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6224839
SamplesNA19472
Known GenesAUH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676899
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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