A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657957



Internal ID9924062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22819936..22824659hg38UCSC Ensembl
Outerchr9:22819779..22824812hg38UCSC Ensembl
Innerchr9:22819935..22824658hg19UCSC Ensembl
Outerchr9:22819778..22824811hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg385034
hg195034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5965205
SamplesHG00689
Known GenesFLJ35282
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657957
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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