A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673463



Internal ID9939568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23005776..23014250hg38UCSC Ensembl
Outerchr9:23005739..23014300hg38UCSC Ensembl
Innerchr9:23005775..23014249hg19UCSC Ensembl
Outerchr9:23005738..23014299hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg388562
hg198562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6533655
SamplesNA19312
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673463
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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