A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668988



Internal ID9935093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4996631..4998561hg38UCSC Ensembl
Outerchr6:4996474..4998714hg38UCSC Ensembl
Innerchr6:4996865..4998795hg19UCSC Ensembl
Outerchr6:4996708..4998948hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382241
hg192241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5702824
SamplesHG00256
Known GenesRPP40
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668988
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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